"Sentinel" Ammonia Ultra Reagent Kit (Non-Sterile) - Taiwan Registration d86f8c60fd47e0c336097500a2bc8137
Access comprehensive regulatory information for "Sentinel" Ammonia Ultra Reagent Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d86f8c60fd47e0c336097500a2bc8137 and manufactured by SENTINEL CH. SPA. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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Device Details
Registration Details
d86f8c60fd47e0c336097500a2bc8137
Ministry of Health Medical Device Import No. 018728
DHA09401872804
Product Details
Limited to the first level identification range of the blood ammonia test system (A.1065) of the management method for medical equipment.
A Clinical chemistry and clinical toxicology
A1065 Blood Ammonia Test System
Imported from abroad
Dates and Status
Jan 17, 2018
Jan 17, 2028

