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

Flexible endoscopic biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100553. The device is manufactured by United States Endoscopy Group, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is STERIS Solutions 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 biopsy forceps, single-use

MHRA Device ID: 100553•Ref: 100553

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Nov 18, 2023

Manufacturer Information

Name

United States Endoscopy Group, Inc.

Address

5976 Heisley Road

Mentor, Ohio, United States

Created Date

Jun 30, 2021

Authorized Representative

Name

STERIS Solutions Limited

Relationship Type

UK Responsible Person

Address

Chancery House, Rayns Way Watermead Business Park Syston

Leicester, Leicestershire, England, United Kingdom

Postcode: LE7 1PF

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

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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