Craniofacial rongeur, single-use - UK MHRA Medical Device Registration

Craniofacial rongeur, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204331. The device is manufactured by Moon Bro (Overseas) Corporation from Pakistan, classified as General Medical Device. The authorized representative in the UK is OXIS INTERNATIONAL 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, single-use

MHRA Device ID: 204331•Ref: 204331

Device Type

General Medical Device

Devices

Craniofacial rongeur, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 1, 2024

Manufacturer Information

Name

Moon Bro (Overseas) Corporation

Address

P.O. Box # 769 Near Railway Gate, Abbot Road

Sialkot, Pakistan

Created Date

Oct 30, 2024

Authorized Representative

Name

OXIS INTERNATIONAL LTD

Relationship Type

UK Responsible Person

Address

4 Latchetts,

Burgess Hill, England, United Kingdom

Postcode: RH15 0YU

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Other Products from Moon Bro (Overseas) Corporation (10)

Other Products from Same Authorized Representative (10)

Craniofacial rongeur, 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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