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 184854. The device is manufactured by HDF Medical (Pvt) Ltd. from Pakistan, classified as General Medical Device. The authorized representative in the UK is Spire Instrumentation 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: 184854•Ref: 184854

Device Type

General Medical Device

Devices

Craniofacial rongeur, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 10, 2024

Manufacturer Information

Name

HDF Medical (Pvt) Ltd.

Address

Head Marala Road, Gohad Pur

Sialkot, Punjab, Pakistan

Created Date

Jan 17, 2024

Authorized Representative

Name

Spire Instrumentation Ltd

Relationship Type

UK Responsible Person

Address

533 Bordesley Green,

Birmingham, England, United Kingdom

Postcode: B9 5XH

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Other Products from HDF Medical (Pvt) Ltd. (10)

Other Products from Same Authorized Representative (10)

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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