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 86536. The device is manufactured by Bactiguard (South East Asia) Sdn. Bhd. (formerly known as VIGILENZ Medical Devices Sdn. Bhd.) from Malaysia, 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: 86536•Ref: 86536

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 27, 2024

Manufacturer Information

Name

Bactiguard (South East Asia) Sdn. Bhd. (formerly known as VIGILENZ Medical Devices Sdn. Bhd.)

Address

308b, Jalan Perindustrian Bukit Minyak 18 Penang Science Park

Simpang Ampat, Penang, Malaysia

Created Date

Jun 26, 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 Bactiguard (South East Asia) Sdn. Bhd. (formerly known as VIGILENZ Medical Devices Sdn. Bhd.) (10)

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

Device Type

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Date Registered

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Address

Created Date

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Relationship Type

Address

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