Flexible endoscopic tissue manipulation forceps, single-use - UK MHRA Medical Device Registration

Flexible endoscopic tissue manipulation forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85886. The device is manufactured by Covidien llc from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic 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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Flexible endoscopic tissue manipulation forceps, single-use

MHRA Device ID: 85886•Ref: 85886

Device Type

General Medical Device

Devices

Flexible endoscopic tissue manipulation forceps, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 28, 2023

Manufacturer Information

Name

Covidien llc

Address

15 Hampshire Street

Mansfield, MA, United States

Created Date

Mar 26, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Flexible endoscopic tissue manipulation forceps, single-use - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

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