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 127842. The device is manufactured by New Ancorvis Srl from Italy, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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 implant suprastructure, temporary, preformed, single-use

MHRA Device ID: 127842•Ref: 127842

Device Type

General Medical Device

Devices

Dental implant suprastructure, temporary, preformed, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Feb 3, 2024

Manufacturer Information

Name

New Ancorvis Srl

Address

Via dell'Industria 15 Bargellino

Bologna, Italy

Created Date

Apr 30, 2021

Authorized Representative

Name

Donawa Lifescience Ltd

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

DJ Fang

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Other Products from New Ancorvis Srl (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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Dental implant suprastructure, permanent, preformed

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Dental implant suprastructure, temporary, preformed, single-use

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