Femur lifter, manual - UK MHRA Medical Device Registration

Femur lifter, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 113709. The device is manufactured by Mizuho OSI from United States, 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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Femur lifter, manual

MHRA Device ID: 113709•Ref: 113709

Device Type

General Medical Device

Devices

Femur lifter, manual

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Mizuho OSI

Address

30031 Ahern Avenue

Union City, United States

Created Date

Nov 18, 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 OSI (10)

Other Products from Same Authorized Representative (10)

Femur lifter, manual - 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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