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 145241. The device is manufactured by W.A. Instruments from Pakistan, classified as General Medical Device. The authorized representative in the UK is HDJ LIMITED.
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Device Type
General Medical Device
Devices
Fistula probe
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Apr 12, 2024
Name
HDJ LIMITEDRelationship Type
Address
16 Churchfields Avenue
Feltham, England, England, United Kingdom
Postcode: Tw135pb
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