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Medical Device Manufacturing Facility

Transforming conceptual designs, existing parts or existing design into practical, high-quality solutions.

From inception to final manufacturing and
commercialization.

we can bring your ideas to life or create customise products & designs to fulfil your requirements.

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Overview

We at KAIRISH Innotech pride ourselves on offering two key services to support your needs. First, we take the time to fully understand your requirements and then develop a fresh, tailored design and concept to meet your needs from inception to final manufacturing and commercialization. Whether you're developing a completely new product or enhancing an existing one, we can bring your ideas to life or create customise products & designs to fulfil your requirements. Alternatively, if you already have a commercialized product, we can assist you in scaling up production by upgrading your existing machinery or developing more advanced equipment to optimize the manufacturing process. Additionally, if you're looking to scale up the production of an existing device, simply provide us with your tech transfer, quality control protocols, and any other relevant details. We'll ensure that the same high standards are maintained throughout the production process.

 

We also offer the flexibility to assemble your existing designs and products in our state-ofthe-art facilities. If preferred, you can transfer your machines to our premises, where we will use our ready-to-use assembly areas to enhance your production capabilities. This seamless integration ensures that you benefit from both advanced infrastructure and expert support.

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Our Custom or Pre Existing 
Technologies For
Commercialization

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Creating a New Design Concept to Final Manufacturing and Commercialization

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Conceptualization and Design Planning

When a customer requests a completely new product, we start with Conceptualization and Design Planning, which serve as the foundation of the medical device development process. It begins with a comprehensive Needs Assessment, where we collaborate closely with healthcare professionals, stakeholders, and customers to thoroughly understand the specific requirements of the medical device. This includes defining its intended use, target market, and any customer-specific needs, ensuring the product will address real-world challenges effectively. Based on this information, we create a detailed Design Brief, which outlines the product’s functional specifications, performance criteria, and regulatory requirements.

The design brief serves as a roadmap for the entire design phase, guiding the team through the process of turning conceptual ideas into tangible, high-quality medical components that meet both customer expectations and industry standards. When working with a pre-existing design or product, we can either assemble, manufacture, or scale it as needed. This includes assembling machines, injection moulding, or simply receiving components and processing them in designated, classified areas.

Image by Kumpan Electric
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Pre-Production Modelling

Our engineers and designers work collaboratively to develop the initial concept of the medical device. This involves careful consideration of factors such as ergonomics, ease of use, material selection, and compatibility with existing medical systems to ensure that the product meets the practical needs of healthcare providers and patients.

 

Once the initial concept is defined, CAD Modelling is employed to create detailed 3D representations of the components using advanced Computer-Aided Design (CAD) software. These digital models provide a visual and functional prototype, allowing for preliminary testing of fit, function, and performance before physical production.

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Material Evaluation

Material Selection and Testing is a critical step in the development of medical components, as the chosen materials directly impact the safety, performance, and longevity of the product. During Material Analysis, we carefully evaluate and select materials that are biocompatible, durable, and appropriate for the specific medical application—whether for drug delivery, injection, reconstitution, or other uses.

Materials such as medical-grade plastics, rubber, and metals are selected as per their proven performance, ability to withstand stress, and compliance with stringent medical standards.

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Materials such as medical-grade plastics, rubber, and metals are selected as per their pro
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Prototype Development

Next, prototyping is carried out using rapid prototyping, or the production of small-scale single-cavity moulds and tools. These techniques allow for early-stage testing and validation of the design's feasibility. This iterative process refines functionality, and ensure the product is ready for the next stage of development.

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Commercial Production & Scape-Up

Once the product design and final prototype are approved, we have the capability to produce all necessary tooling and machinery—whether semi-automatic or fully automatic—entirely in-house. Our facilities are equipped with dedicated areas for machine installation, offering us great flexibility in customizing setups based on customer needs. We can begin with lowoutput machines for initial production runs and progressively scale up to high-output or mass-production systems as required.

We integrate stringent Quality Control procedures at every stage of the process to identify and rectify any deviations, ensuring that each product meets our high standards. Our cleanroom is certified according to ISO 14644 standards, ensuring a controlled environment that meets the highest levels of cleanliness and safety. This controlled environment minimizes the risk of contamination, especially for devices that will come into direct contact with patients or drug products. We can also operate our machines under Laminar Air Flow (LAF) system.

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Regulatory Conformance &
Site Approvals

Regulatory Compliance and Validation are central to our medical device manufacturing process, ensuring that all medical devices meet the highest standards of safety, efficacy, and quality

 

To comply with regulatory requirements, we prepare and maintain detailed documentation for each product. This includes-Design History Files (DHFs), Device Master Records (DMRs), Risk Management Files.

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To comply with regulatory requirements, we prepare and maintain detailed documentation for each product. This includes-Design History Files (DHFs), Device Master Records (DMRs), Risk Management Files.

 

These documents provide a clear traceability record, demonstrating that each product has undergone rigorous testing and validation to meet regulatory requirements. They also ensure that the devices we produce are safe for their intended use and perform as expected. Certified by ISO 9001:2015 and ISO 13485:2016, which govern quality management and risk management practices throughout the design and manufacturing phases. These certifications confirm our commitment to consistent product quality and operational excellence.

In addition to ISO standards, we are also audited & approved by CDSCO (Central Drugs Standard Control Organisation) for the sterile medical devices that we produce currently. We prepare comprehensive documentation to demonstrate that each product meets the stringent safety, performance, and regulatory requirements. Our Design Validation and Verification processes are critical to ensuring that the product meets its intended use and safety requirements.

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These documents provide a clear traceability record, demonstrating that each product has undergone rigorous testing and validation to meet regulatory requirements. They also ensure that the devices we produce are safe for their intended use and perform as expected.

 

Certified by ISO 9001:2015 and ISO 13485:2016, which govern quality management and risk management practices throughout the design and manufacturing phases. These certifications confirm our commitment to consistent product quality and operational excellence.

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In addition to ISO standards, we are also audited & approved by CDSCO (Central Drugs Standard Control Organisation) for the sterile medical devices that we produce currently. We prepare comprehensive documentation to demonstrate that each product meets the stringent safety, performance, and regulatory requirements.

 

Our Design Validation and Verification processes are critical to ensuring that the product meets its intended use and safety requirements.

Advance Enginnering & Design

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Image by Kumpan Electric

Material Selection

We leverage machine learning technology to ensure precise data analysis and research.

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Alloy Forte

Coatings

PMI

Supported Net Zero Families by 2035

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Monthly Business Net Zero Conversions

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Sponsor Net Zero Scholars by 2035

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Material Selection Expertise

As a custom parts and components manufacturer, the ability to select and work with a variety of materials—metals, plastics, composites, and alloys—is our forte. We understand the properties of materials (strength, hardness, heat resistance, corrosion resistance etc.) which is essential for choosing the right material for each application.

Material Selection Expertise

As a custom parts and components manufacturer, the ability to select and work with a variety of materials—metals, plastics, composites, and alloys—is our forte. We understand the properties of materials (strength, hardness, heat resistance, corrosion resistance etc.) which is essential for choosing the right material for each application.

Screenshot 2025-08-28 at 7.51.39 PM.png

As a custom parts and components manufacturer, the ability to select and work with a variety of materials—metals, plastics, composites, and alloys—is our forte. We understand the properties of materials (strength, hardness, heat resistance, corrosion resistance etc.) which is essential for choosing the right material for each application.

Flexible Production Capacity

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Flexible Production Capacity

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1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.

Flexible Production Capacity

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Flexible Production Capacity

Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the

1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.

Flexible Production Capacity

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Materials Expertise

As a custom parts and components manufacturer, the ability to select and work with a variety of materials—metals, plastics, composites, and alloys—is our forte. 

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Quality Assurance

We understand the properties of materials (strength, hardness, heat resistance, corrosion resistance etc.) which is essential for choosing the right material for each application.
We provide Advanced Coatings & Treatments whenever necessary.

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Specialized Finishing

We leverage a PMI (Positive Material Identification) gun in our manufacturing processes which oers immediate feedback, allowing us to identify and address material discrepancies on the spot, saving time compared to sending samples to a lab & ensuring that the material so received, matches the exact specifications and technical requirements of what has been ordered.

Manufacturing Process

Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.

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CNC MACHINING

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TURNING AND MILLING

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GRINDING

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INJECTION MOULD
MANUFACTURING

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dadachanji_pattern
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Manufacturing Process

When providing high-quality custom engineering and parts solutions, we partner with you to configure our production plant to your unique specifications.

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TURNING &
MILLING

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GRINDING

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CNC MACHINE

01

MANUFACTURING & CAPABILITIES

VMC

MACHINES

Equipped with eight Vertical Machining Centers (VMCs) from HAAS & DMG Mori, featuring both 3-axis and 4-axis capabilities. 

These machines allow us to manufacture intricate and complex parts with exceptional precision.

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02

MANUFACTURING & CAPABILITIES

TURN-MILL

CENTRE

Designed for producing cylindrical and concentric parts, this machine also performs light milling operations.

This makes it an ideal for precision threading and multi-functional machining.

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03

MANUFACTURING & CAPABILITIES

CNC EDM (Electrical Discharge Machining)

Our EDM machine uses electrical sparks to erode material, enabling the creation of intricate shapes, cavities, and fine details.

This specialized process has been meticulously designed and implemented to ensure that every single part we create meets an exceptional level of superior precision.

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CNC EDM..heic

04

MANUFACTURING & CAPABILITIES

CNC

Wire Cut

Our Chmer wire cutting machine operates with an ultra-thin 0.25 mm wire, delivering precise cuts on steel, aluminum, and copper with an accuracy of up to 5 microns.

This specialized process has been meticulously designed and implemented to ensure that every single part we create meets an exceptional level of superior precision.

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05

MANUFACTURING & CAPABILITIES

GRINDING

Designed to maintain outer diameter (OD) and inner diameter (ID) accuracy in cylindrical workpiece or a flat surface as well.

Achieves concentricity below 0.002 mm and dimensional accuracy up to 0.005 microns.

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06

MANUFACTURING & CAPABILITIES

LAZER

WELDING

Our laser welding machine delivers precise, high-strength, and clean welds, 

This ensures superior durability and accuracy in component fabrication.

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Manufacturing Process

When providing high-quality custom engineering and parts solutions, we partner with you to configure our production plant to your unique specifications.

Screenshot 2025-08-22 at 4.27.52 PM.png

TURNING &
MILLING

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GRINDING

CNC machining process.jpg

CNC MACHINE

01

MANUFACTURING & CAPABILITIES

VMC Machines

Equipped with eight Vertical Machining Centers (VMCs) from HAAS & DMG Mori, featuring both 3-axis and 4-axis capabilities.

These machines allow us to manufacture intricate and complex parts with exceptional precision.

Read More

CNC machining process.jpg

02

MANUFACTURING & CAPABILITIES

Grinding

Designed to maintain outer diameter (OD) and inner diameter (ID) accuracy in cylindrical workpiece or a flat surface as well.

Achieves concentricity below 0.002 mm and dimensional accuracy up to 0.005 microns.

Read More

CNC machining process.jpg

03

MANUFACTURING & CAPABILITIES

CNC EDM (Electrical Discharge Machining)

Utilizing electrical sparks to erode material, our EDM machine

Enabling the creation of
intricate shapes, cavities, and fine details, ensuring superior precision.

Read More

CNC machining process.jpg

04

MANUFACTURING & CAPABILITIES

Turning & Milling

Designed for producing cylindrical and concentric parts, this machine also performs light
milling operations.

Hence making it ideal for precision threading and multi-functional machining.

Read More

CNC machining process.jpg

05

MANUFACTURING & CAPABILITIES

CNC Wire Cut

Our Chmer wire cutting machine operates with an ultra-thin 0.25 mm wire.

Delivering precise
cuts on steel, aluminum, and copper with an accuracy of up to 5 microns.

Read More

CNC machining process.jpg

06

MANUFACTURING & CAPABILITIES

Laser Welding

Our laser welding machine delivers precise, high-strength, and clean welds.

This ensures superior durability and accuracy in component fabrication.

Read More

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Conventional Machining

When providing high-quality custom engineering and parts solutions, we partner with you to configure our production plant to your unique specifications.

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DRILLING

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LATHE

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MILLING

CNC EDM..heic

01

CONVENTIONAL

MACHINING

DRILLING

Enables precise hole-making across various materials.

This process ensures accuracy and efficiency in component manufacturing.

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02

CONVENTIONAL

MACHINING

LATHE

Facilitates precision turning, cutting, and shaping of materials for high-accuracy, high-quality component production.

This makes it an ideal for precision threading and multi-functional machining.

Read More

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03

CONVENTIONAL

MACHINING

MILLING

Performs precision cutting, shaping, and finishing, ensuring superior accuracy and consistency in manufacturing.

This specialized process has been meticulously designed and implemented to ensure that every single part we create meets an exceptional level of superior precision.

Read More

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Customisation & Flexibility

Offering fully customised solutions that meet the specific design and operational needs of clients. We offer a wide range of materials (SS, MS, Brass, Copper, Aluminium, Plastics, composites) to meet performance criteria, including strength, durability, and corrosion resistance.

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01

Flexible Production Capacity

Ensuring our facility to adapt to varying orders, whether for prototypes, low-volume runs, or large-scale production, we are equipped to support various industry sectors.

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02

Rapid Prototyping & Iterations

Our ability to quickly develop and iterate on prototypes allows clients to see the potential design in action and make modifications early in the development cycle.

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03

Quality Control & Testing

 Utilising tools like coordinate measuring machines (CMMs), 3D scanners, and Vision Measuring Machines (VMMs) to measure the dimensions and tolerances of parts with high accuracy.

Customisation & Flexibility

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Customisation & Flexibility

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Customisation & Flexibility

Image by Jakub Żerdzicki

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Customisation & Flexibility

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Quality Control & Final Inspection

Quality Control and Final Inspection are integral parts of our manufacturing process, ensuring that every product meets the highest standards of safety and performance. In the final stage of production, each product undergoes a rigorous Inspection and Testing process, which includes detailed visual inspections, dimensional checks, and functionality tests. These procedures are designed to confirm that every component adheres to the required specifications and complies with regulatory standards.

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Scaling Up Production for an Existing Commercialized Product

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Tech Transfer

If our customers already have an existing design and a smaller manufacturing setup, or if they wish to transfer their operations to an external facility, we have already set up dedicated spaces to facilitate this transition smoothly. Additionally, we can set up larger machines as an
alternative site to complement or scale up their current production, ensuring a smooth and efficient transfer of operations.
It begins with receiving detailed design documentation, including technical drawings, specifications, material lists, and quality control (QC) guidelines. This information serves as the foundation for replicating the product with high accuracy. Next, we review the client’s existing manufacturing processes, carefully analyzing each step to identify potential areas
for improvement and ensure alignment with the latest industry best practices. Finally, we assess the client’s current QC protocols, ensuring they are robust and well-implemented for the scaled-up production. This thorough evaluation guarantees that product quality remains
consistent, and any necessary adjustments are made to accommodate higher volumes while maintaining compliance with regulatory standards.

AI Images.jpg
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Regulatory Conformance &
Site Approvals

Regulatory Compliance and Validation are central to our medical device manufacturing process, ensuring that all medical devices meet the highest standards of safety, efficacy, and quality

 

To comply with regulatory requirements, we prepare and maintain detailed documentation for each product. This includes-Design History Files (DHFs), Device Master Records (DMRs), Risk Management Files.

Screenshot 2025-10-18 at 10.37.41 PM.png
dadachanji_pattern_edited_edited.png

These documents provide a clear traceability record, demonstrating that each product has undergone rigorous testing and validation to meet regulatory requirements. They also ensure that the devices we produce are safe for their intended use and perform as expected.

 

Certified by ISO 9001:2015 and ISO 13485:2016, which govern quality management and risk management practices throughout the design and manufacturing phases. These certifications confirm our commitment to consistent product quality and operational excellence.

Screenshot 2025-10-18 at 10.37.55 PM.png
Screenshot 2025-10-18 at 10.38.01 PM.png

In addition to ISO standards, we are also audited & approved by CDSCO (Central Drugs Standard Control Organisation) for the sterile medical devices that we produce currently. We prepare comprehensive documentation to demonstrate that each product meets the stringent safety, performance, and regulatory requirements.

 

Our Design Validation and Verification processes are critical to ensuring that the product meets its intended use and safety requirements.

dadachanji_pattern_edited_edited.png

Quality Control & Final Inspection

Quality Control and Final Inspection are integral parts of our manufacturing process, ensuring that every product meets the highest standards of safety and performance. In the final stage of production, each product undergoes a rigorous Inspection and Testing process, which includes detailed visual inspections, dimensional checks, and functionality tests. These procedures are designed to confirm that every component adheres to the required specifications and complies with regulatory standards.

IMG_1371.JPG
dadachanji_pattern_edited.png
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Untitled design-2.png

Supply Chain &
Inventory Management

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Operational Scale of our
Medical Device Facility

Our medical device manufacturing facility is split into various areas which collectively spans an impressive 26,000 square feet, providing a premier environment for the design, development, and production of high-quality medical devices. This expansive space spans two dedicated floors, each equipped with ISO 14644 certified cleanrooms, fully prepared to accommodate equipment and start production swiftly.

Additionally, we have a separate, specialized area for in-house ETO sterilization, ensuring streamlined and efficient manufacturing capabilities. The large scale of our facility enables us to accommodate highvolume production while maintaining strict adherence to industry standards and regulatory requirements.

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“ We received a unique request from one of our customers, who presented us with a product

concept they wanted to develop, from there, we did it all—from sourcing materials in the USand refining the design, to creating injection moulds and manufacturing components in- house. We even built the assembly machine ourselves, handled sterilization, and packed the products. But we didn’t stop there! We went the extra mile by designing and building a fully customized

final packing line where our product is combined & packed with the customer’s product. And,

in the end, we continued to deliver millions of pieces! Talk about going the extra mile!  ”

Knowledge
Nuggets

“ Did you know we offer sterile medical devices with the highest safety standards? We’ve got

you covered with flexible sterilization options—whether it's in-house ETO, steam sterilization,

or external Gamma sterilization—whatever suits the part or your preferences best! ”

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