Rigid endoscopic tissue manipulation forceps, reusable - UK MHRA Medical Device Registration

Rigid endoscopic tissue manipulation forceps, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100438. The device is manufactured by Stryker Endoscopy, a division of Stryker Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Stryker 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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Rigid endoscopic tissue manipulation forceps, reusable

MHRA Device ID: 100438•Ref: 100438

Device Type

General Medical Device

Devices

Rigid endoscopic tissue manipulation forceps, reusable

Type

Class IIb

Date Registered

Sep 24, 2024

Last Updated

Dec 21, 2023

Manufacturer Information

Name

Stryker Endoscopy, a division of Stryker Corporation

Address

5900 Optical Ct

San Jose, United States

Created Date

Mar 17, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Rigid endoscopic tissue manipulation forceps, reusable - UK MHRA Medical Device Registration

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