Manual external defibrillator - UK MHRA Medical Device Registration

Manual external defibrillator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178580. The device is manufactured by WEINMANN Emergency Medical Technology GmbH + Co.KG 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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Manual external defibrillator

MHRA Device ID: 178580•Ref: 178580

Device Type

General Medical Device

Devices

Manual external defibrillator

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

WEINMANN Emergency Medical Technology GmbH + Co.KG

Address

Frohbösestraße 12

Hamburg, Hamburg, Germany

Created Date

Jul 16, 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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Other Products from WEINMANN Emergency Medical Technology GmbH + Co.KG (10)

Other Products from Same Authorized Representative (10)

Manual external defibrillator - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

Name

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Address

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