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 121965. The device is manufactured by Olympus Winter & IBE from Germany, classified as General Medical Device. The authorized representative in the UK is KeyMed (Medical & Industrial Equipment) Ltd..

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Endometrial biopsy curette

MHRA Device ID: 121965•Ref: 121965

Device Type

General Medical Device

Devices

Endometrial biopsy curette

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 2, 2024

Manufacturer Information

Name

Olympus Winter & IBE

Address

Kuehnstraße 61

Hamburg, Germany

Created Date

May 17, 2021

Authorized Representative

Name

KeyMed (Medical & Industrial Equipment) Ltd.

Relationship Type

UK Responsible Person

Address

Keymed House Stock Road

Southend-on-sea, Essex, United Kingdom

Postcode: SS2 5QH

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Endometrial biopsy curette - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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