Pure Global

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.

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.

Free Database
Powered by Pure Global AI
MHRA Registered
General Medical Device
๐Ÿ‡ฌ๐Ÿ‡ง
Polyolefin/fluoropolymer suture, multifilament
MHRA Device ID: 81213โ€ขRef: 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

Address

16597 N. 92nd St. 101 Scottsdale

Scottsdale , Arizona , United States

Created Date

May 18, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing