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 163682. The device is manufactured by Ritter Implants GmbH & Co.KG from Germany, classified as General Medical Device. The authorized representative in the UK is Medes Ltd..

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

MHRA Device ID: 163682•Ref: 163682

Device Type

General Medical Device

Devices

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

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 15, 2024

Manufacturer Information

Name

Ritter Implants GmbH & Co.KG

Address

Freiburger Straße 45

Biberach, Germany

Created Date

Dec 22, 2022

Authorized Representative

Name

Medes Ltd.

Relationship Type

UK Responsible Person

Address

5 Beaumont Gate, Shenley Hil

Radlett, Herts, England, United Kingdom

Postcode: WD77AR

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

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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