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 102794. The device is manufactured by Purgo Biologics Inc. from South Korea, classified as General Medical Device. The authorized representative in the UK is Obelis UK Ltd.

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, monofilament

MHRA Device ID: 102794•Ref: 102794

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 27, 2024

Manufacturer Information

Name

Purgo Biologics Inc.

Address

#812 27 Dunchon-daero 457beon-gil Jungwon-gu

Seongnam-si, Gyeonggi-do, South Korea

Created Date

Sep 6, 2021

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

DJ Fang

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Other Products from Purgo Biologics Inc. (1)

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Type: General Medical Device

Registered: Nov 26, 2024

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

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