Fistula probe - UK MHRA Medical Device Registration

Fistula probe is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 152890. The device is manufactured by Buraq Surgical Corporation from Pakistan, classified as General Medical Device. The authorized representative in the UK is AF PHARMA SERVICE UK 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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Fistula probe

MHRA Device ID: 152890•Ref: 152890

Device Type

General Medical Device

Devices

Fistula probe

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 21, 2023

Manufacturer Information

Name

Buraq Surgical Corporation

Address

59-C Industrial Estate

Sialkot, Pakistan

Created Date

Jul 27, 2022

Authorized Representative

Name

AF PHARMA SERVICE UK LTD

Relationship Type

UK Responsible Person

Address

Suite 140 Temple Chambers 3-7 Temple Avenue

London, England, United Kingdom

Postcode: EC4Y 0DA

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Other Products from Buraq Surgical Corporation (10)

Other Products from Same Authorized Representative (10)

Fistula probe - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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