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

Dental/maxillofacial surgical procedure kit, non-medicated, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 73620. The device is manufactured by Institut Straumann AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is Straumann Ltd.

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, single-use
MHRA Device ID: 73620Ref: 73620

Device Type

General Medical Device

Devices

Dental/maxillofacial surgical procedure kit, non-medicated, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Feb 15, 2024

Manufacturer Information

Address

Peter Merian-Weg 12,

CH-4002 Basel,, CH-4002 Basel, Switzerland

Created Date

Mar 16, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

10 Finsbury Square

London, England, United Kingdom

Postcode: EC2A 1AF

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