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 77801. The device is manufactured by MANI, INC. from Japan, 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: 77801•Ref: 77801

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Feb 28, 2024

Manufacturer Information

Name

MANI, INC.

Address

8-3 Kiyohara Industrial Park

Utsunomiya, Tochigi, Japan

Created Date

Apr 29, 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

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Other Products from MANI, INC. (10)

Other Products from Same Authorized Representative (10)

Polyolefin/fluoropolymer suture, monofilament - 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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