Craniofacial rongeur, reusable - UK MHRA Medical Device Registration

Craniofacial rongeur, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 157299. 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.

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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Craniofacial rongeur, reusable

MHRA Device ID: 157299•Ref: 157299

Device Type

General Medical Device

Devices

Craniofacial rongeur, reusable

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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Other Products from KLS Martin SE & Co. KG (10)

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Craniofacial rongeur, 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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