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.
Device Type
General Medical Device
Devices
Polyolefin/fluoropolymer suture, multifilament
Type
Class IIb
Date Registered
Apr 11, 2024
Last Updated
Mar 22, 2024
Name
Cayenne MedicalAddress
16597 N. 92nd St. 101 Scottsdale
Scottsdale , Arizona , United States
Created Date
May 18, 2021
Relationship Type
Address
Stella Building Windmill Hill Business Park Whitehill Way
Swindon, England, United Kingdom
Postcode: SN5 6NX
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