Maxillofacial bone separator - UK MHRA Medical Device Registration

Maxillofacial bone separator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 123915. The device is manufactured by Rex Implants 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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Maxillofacial bone separator

MHRA Device ID: 123915•Ref: 123915

Device Type

General Medical Device

Devices

Maxillofacial bone separator

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Aug 23, 2024

Manufacturer Information

Name

Rex Implants

Address

850 Michigan Avenue

Columbus, Ohio, United States

Created Date

Aug 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

DJ Fang

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Maxillofacial bone separator - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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