Bone access cannula - UK MHRA Medical Device Registration

Bone access cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 109110. The device is manufactured by Ranfac Corporation 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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Bone access cannula

MHRA Device ID: 109110

Device Type

General Medical Device

Devices

Bone access cannula

Type

Class IIa

Date Registered

Oct 20, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Ranfac Corporation

Address

30 Doherty Avenue

Avon, Massachusetts, United States

Created Date

Oct 20, 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 Ranfac Corporation (5)

Other Products from Same Authorized Representative (10)

Bone access cannula - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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