Dental implant suprastructure, temporary, preformed, single-use - UK MHRA Medical Device Registration

Dental implant suprastructure, temporary, preformed, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163680. 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 implant suprastructure, temporary, preformed, single-use

MHRA Device ID: 163680•Ref: 163680

Device Type

General Medical Device

Devices

Dental implant suprastructure, temporary, preformed, single-use

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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Other Products from Ritter Implants GmbH & Co.KG (10)

Other Products from Same Authorized Representative (10)

Dental implant suprastructure, temporary, preformed, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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