Polyolefin/fluoropolymer suture, monofilament - UK MHRA Medical Device Registration

Polyolefin/fluoropolymer suture, monofilament is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 77667. 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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Polyolefin/fluoropolymer suture, monofilament

MHRA Device ID: 77667•Ref: 77667

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class III

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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Polyolefin/fluoropolymer suture, monofilament - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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