Dental/maxillofacial surgical procedure kit, non-medicated, reusable - UK MHRA Medical Device Registration

Dental/maxillofacial surgical procedure kit, non-medicated, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89172. The device is manufactured by BioHorizons Implant Systems, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Adveniunt Medical International Limited (trading as Quality First International).

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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Dental/maxillofacial surgical procedure kit, non-medicated, reusable

MHRA Device ID: 89172•Ref: 89172

Device Type

General Medical Device

Devices

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Type

Class IIa

Date Registered

May 24, 2020

Last Updated

Oct 13, 2022

Manufacturer Information

Name

BioHorizons Implant Systems, Inc.

Address

2300 Riverchase Center

Birmingham, Alabama, United States

Created Date

May 24, 2020

Authorized Representative

Name

Adveniunt Medical International Limited (trading as Quality First International)

Relationship Type

UK Responsible Person

Address

1 Cooks Road Stratford

London, England, United Kingdom

Postcode: E15 2PW

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Dental/maxillofacial surgical procedure kit, non-medicated, reusable - UK MHRA Medical Device Registration

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Date Registered

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