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 174174. The device is manufactured by Apollo Endosurgery, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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Device Type
General Medical Device
Devices
Polyolefin/fluoropolymer suture, monofilament
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Oct 18, 2024
Address
1120 S Capital of Texas Hwy
Austin, Texas, United States
Created Date
Nov 10, 2021
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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