Endometrial biopsy curette - UK MHRA Medical Device Registration

Endometrial biopsy curette is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 154396. The device is manufactured by Gimmi 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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Endometrial biopsy curette

MHRA Device ID: 154396•Ref: 154396

Device Type

General Medical Device

Devices

Endometrial biopsy curette

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 2, 2024

Manufacturer Information

Name

Gimmi GmbH

Address

Carl-Zeiss-Straße 6

Tuttlingen, Germany

Created Date

Aug 23, 2021

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 Gimmi GmbH (10)

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Endometrial biopsy curette - 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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