Periodontal file/rasp, manual - UK MHRA Medical Device Registration

Periodontal file/rasp, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 157310. The device is manufactured by KLS Martin SE & Co. KG from Germany, classified as General Medical Device. The authorized representative in the UK is confinis (UK) RP Ltd.

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Periodontal file/rasp, manual

MHRA Device ID: 157310•Ref: 157310

Device Type

General Medical Device

Devices

Periodontal file/rasp, manual

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 6, 2024

Manufacturer Information

Name

KLS Martin SE & Co. KG

Address

KLS Martin Platz 1

Tuttlingen, Germany

Created Date

Sep 30, 2022

Authorized Representative

Name

confinis (UK) RP Ltd

Relationship Type

UK Responsible Person

Address

St John's Innovation Centre Cowley Road

Cambridge, England, United Kingdom

Postcode: CB4 0WS

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Periodontal file/rasp, manual - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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