Taiwan FDA registration 11f3be00b79adb9432bc2cac0ed96ee8

Maxe blood alcohol/ammonia test liquid quality control group

TW: 麥斯血中酒精/氨檢測液狀品管組

Taiwan·Risk Class 2·MICROGENICS CORPORATION·Registered Mar 05, 2021 – Mar 05, 2026Expired

Registration details

Analysis ID: 11f3be00b79adb9432bc2cac0ed96ee8
Customs Code: DHA05603437001

Company information

Manufacturer: MICROGENICS CORPORATION
Manufacturer Country: United States
Authorized Representative: THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.

Product details

Intended Use: This product is used in clinical laboratories as a quantitative solution to monitor assays for the determination of alcohol and/or ammonia in human serum and/or plasma samples.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Quality control materials (analytical and non-analytical)
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Mar 05, 2021
Expiry Date: Mar 05, 2026

About this record

Access comprehensive regulatory information for Maxe blood alcohol/ammonia test liquid quality control group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11f3be00b79adb9432bc2cac0ed96ee8 and manufactured by MICROGENICS CORPORATION. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..

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