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 110871. The device is manufactured by Medi-Globe GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Flexible endoscopic biopsy forceps, single-use

MHRA Device ID: 110871•Ref: 110871

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Medi-Globe GmbH

Address

Medi-Globe Straße 1-5

Achenmühle, Germany

Created Date

Apr 13, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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

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Last Updated

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Created Date

Name

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DJ Fang

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