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

Whole-blood-recovery autotransfusion system, powered is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 101151. The device is manufactured by Teleflex Medical from United States, classified as General Medical Device. The authorized representative in the UK is TFX Group Ltd.

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Whole-blood-recovery autotransfusion system, powered

MHRA Device ID: 101151•Ref: 101151

Device Type

General Medical Device

Devices

Whole-blood-recovery autotransfusion system, powered

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 12, 2024

Manufacturer Information

Name

Teleflex Medical

Address

3015 Carrington Mill Boulevard

Morrisville, North Carolina, United States

Created Date

Apr 22, 2021

Authorized Representative

Name

TFX Group Ltd

Relationship Type

UK Responsible Person

Address

Grosvenor House Horseshoe Crescent

Old Town Beaconsfield, England, United Kingdom

Postcode: HP9 1LJ

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Other Products from Teleflex Medical (10)

Other Products from Same Authorized Representative (10)

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

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Date Registered

Last Updated

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Address

Created Date

Name

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DJ Fang

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