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 200441. The device is manufactured by Camark SA from Greece, classified as General Medical Device. The authorized representative in the UK is STERIS Solutions Limited.

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Polyolefin/fluoropolymer suture, monofilament

MHRA Device ID: 200441•Ref: 200441

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 25, 2024

Manufacturer Information

Name

Camark SA

Address

Industrial Park Axioupoli

Axioupoli, Greece

Created Date

Oct 27, 2022

Authorized Representative

Name

STERIS Solutions Limited

Relationship Type

UK Responsible Person

Address

Chancery House, Rayns Way Watermead Business Park Syston

Leicester, Leicestershire, England, United Kingdom

Postcode: LE7 1PF

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

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