General-purpose curette - UK MHRA Medical Device Registration

General-purpose curette is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 177668. The device is manufactured by MIZUHO Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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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General-purpose curette

MHRA Device ID: 177668•Ref: 177668

Device Type

General Medical Device

Devices

General-purpose curette

Type

Class I

Date Registered

Sep 24, 2024

Last Updated

May 22, 2024

Manufacturer Information

Name

MIZUHO Corporation

Address

3-30-13 Hongo Bunkyo-ku

Tokyo, Japan

Created Date

May 24, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Other Products from MIZUHO Corporation (10)

Other Products from Same Authorized Representative (10)

General-purpose curette - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

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Address

DJ Fang

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