Bone file/rasp, manual, reusable - UK MHRA Medical Device Registration

Bone file/rasp, manual, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 153203. The device is manufactured by FENTEX medical GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL UK LIMITED.

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Bone file/rasp, manual, reusable

MHRA Device ID: 153203•Ref: 153203

Device Type

General Medical Device

Devices

Bone file/rasp, manual, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jan 16, 2024

Manufacturer Information

Name

FENTEX medical GmbH

Address

take-off GewerbePark 2

Neuhausen ob Eck, Baden-Württemberg, Germany

Created Date

Jul 22, 2022

Authorized Representative

Name

MEDAGENT INTERNATIONAL UK LIMITED

Relationship Type

UK Responsible Person

Address

2 St Andrews Place

Lewes, East Sussex, England, United Kingdom

Postcode: BN7 1UP

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Other Products from FENTEX medical GmbH (10)

Other Products from Same Authorized Representative (10)

Bone file/rasp, manual, reusable - 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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