Ammonia IVD, reagent - UK MHRA Medical Device Registration
Ammonia IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 196854. The device is manufactured by Fisher Diagnostics Inc. from United States, classified as In Vitro Diagnostic Device.
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Device Type
In Vitro Diagnostic Device
Type
Class C
Status
Date Registered
Jul 11, 2024
Address
Fisher Diagnostics Inc., 8365 Valley Pike
Middletown, Virginia, United States
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