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

Polyolefin/fluoropolymer suture, multifilament is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 81213. The device is manufactured by Cayenne Medical from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet UK Limited.

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Polyolefin/fluoropolymer suture, multifilament

MHRA Device ID: 81213•Ref: 81213

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, multifilament

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Mar 22, 2024

Manufacturer Information

Name

Cayenne Medical

Address

16597 N. 92nd St. 101 Scottsdale

Scottsdale , Arizona , United States

Created Date

May 18, 2021

Authorized Representative

Name

Zimmer Biomet UK Limited

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

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

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

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DJ Fang

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