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 102158. The device is manufactured by Riverpoint Medical, LLC from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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.

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Polyolefin/fluoropolymer suture, multifilament

MHRA Device ID: 102158•Ref: 102158

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, multifilament

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Sep 26, 2024

Manufacturer Information

Name

Riverpoint Medical, LLC

Address

825 NE 25th Ave

Portland, Oregon, United States

Created Date

Sep 1, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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