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 106344. The device is manufactured by PHEASANT SURGICAL CORPORATION from Pakistan, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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: 106344•Ref: 106344

Device Type

General Medical Device

Devices

Craniofacial rongeur, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jun 6, 2024

Manufacturer Information

Name

PHEASANT SURGICAL CORPORATION

Address

786 # NAI ABADI MURAD PUR

SIALKOT, Pakistan

Created Date

Aug 15, 2021

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Craniofacial rongeur, reusable - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

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