Endomyocardial biopsy forceps, single-use - UK MHRA Medical Device Registration

Endomyocardial biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178295. The device is manufactured by H. + H. Maslanka Chirurgische Instrumente GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL UK 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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Endomyocardial biopsy forceps, single-use

MHRA Device ID: 178295•Ref: 178295

Device Type

General Medical Device

Devices

Endomyocardial biopsy forceps, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jun 22, 2024

Manufacturer Information

Name

H. + H. Maslanka Chirurgische Instrumente GmbH

Address

Stockacher Strasse 172

Tuttlingen, Germany

Created Date

Sep 1, 2023

Authorized Representative

Name

MEDAGENT INTERNATIONAL UK LIMITED

Relationship Type

UK Responsible Person

Address

2 St Andrews Place

Lewes, East Sussex, England, United Kingdom

Postcode: BN7 1UP

DJ Fang

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Other Products from H. + H. Maslanka Chirurgische Instrumente GmbH (3)

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Endomyocardial biopsy forceps, single-use - 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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