United Kingdom MHRA device registration 81213

Polyolefin/fluoropolymer suture, multifilament

United Kingdom·General Medical Device·Cayenne Medical·Registered Apr 11, 2024

Registration details

Device ID: 81213
MHRA Reference Number: 81213
Date Registered: Apr 11, 2024
Last Updated: Mar 22, 2024

Device classification

Device Type: General Medical Device
Devices: Polyolefin/fluoropolymer suture, multifilament
Type: Class IIb

Manufacturer

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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About this record

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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