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 70909. The device is manufactured by ACME COMMERCIAL WAYS (PVT) LTD from Pakistan, classified as General Medical Device. The authorized representative in the UK is HDJ LIMITED.

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: 70909•Ref: 70909

Device Type

General Medical Device

Devices

Fistula probe

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 18, 2024

Manufacturer Information

Name

ACME COMMERCIAL WAYS (PVT) LTD

Address

P.O. Box # 1092

sialkot, Pakistan

Created Date

Mar 29, 2021

Authorized Representative

Name

HDJ LIMITED

Relationship Type

UK Responsible Person

Address

16 Churchfields Avenue

Feltham, England, England, United Kingdom

Postcode: Tw135pb

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Other Products from ACME COMMERCIAL WAYS (PVT) LTD (10)

Other Products from Same Authorized Representative (10)

Fistula probe - 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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Fistula probe

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Instrument tray, reusable

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