Whole-blood-recovery autotransfusion system, manual - UK MHRA Medical Device Registration

Whole-blood-recovery autotransfusion system, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135675. The device is manufactured by Stryker Instruments, a division of Stryker Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Stryker UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Whole-blood-recovery autotransfusion system, manual

MHRA Device ID: 135675•Ref: 135675

Device Type

General Medical Device

Devices

Whole-blood-recovery autotransfusion system, manual

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 7, 2023

Manufacturer Information

Name

Stryker Instruments, a division of Stryker Corporation

Address

4100 E. Milham Ave

Kalamazoo, Michigan, United States

Created Date

Mar 3, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Whole-blood-recovery autotransfusion system, manual - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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