Endoscope antifog solution - UK MHRA Medical Device Registration
Endoscope antifog solution is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 52991. The device is manufactured by LaproSurge Ltd from England, United Kingdom, classified as General Medical Device.
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Device Type
General Medical Device
Devices
Endoscope antifog solution
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Mar 2, 2024
Name
LaproSurge LtdAddress
Unit 5b Fisher Industrial Estate Wiggenhall Road
Watford, Hertfordshire, England, United Kingdom
Created Date
Aug 29, 2019
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