Cardioplegia solution administration kit - UK MHRA Medical Device Registration
Cardioplegia solution administration kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 212281. The device is manufactured by Quest Medical, Inc. from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class IIa
Status
Date Registered
Mar 4, 2025
Address
1 Allentown Parkway
Allen, Texas, United States
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