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Apibeta barbital test group - Taiwan Registration f0a848e2a3b6a634b4490317717dd03a

Access comprehensive regulatory information for Apibeta barbital test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0a848e2a3b6a634b4490317717dd03a and manufactured by B.R.A.H.M.S GmbH;; MICROGENICS CORPORATION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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f0a848e2a3b6a634b4490317717dd03a
Registration Details
Taiwan FDA Registration: f0a848e2a3b6a634b4490317717dd03a
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Device Details

Apibeta barbital test group
TW: ไบžๅŸน่‹ฏๅŸบๅทดๆฏ”ๅฆฅๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

f0a848e2a3b6a634b4490317717dd03a

DHA05603312302

Company Information

Product Details

This product is used for the in vitro quantitative detection of phenylbarbital in human serum or plasma on the Alinity c analyzer.

A Clinical chemistry and clinical toxicology

A.3660 ่‹ฏๅŸบๅทดๆฏ”ๅฆฅ่ฉฆ้ฉ—็ณป็ตฑ

Input;; Contract manufacturing

Dates and Status

Jan 06, 2020

Jan 06, 2030