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"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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d86f8c60fd47e0c336097500a2bc8137
Registration Details
Taiwan FDA Registration: d86f8c60fd47e0c336097500a2bc8137
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Device Details

"Sentinel" Ammonia Ultra Reagent Kit (Non-Sterile)
TW: "่–ๆ่ซพ"่ก€ๆฐจๆชข้ฉ—่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d86f8c60fd47e0c336097500a2bc8137

Ministry of Health Medical Device Import No. 018728

DHA09401872804

Company Information

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