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“Abbott” SHBG Reagent Kit (Non-Sterile) - Taiwan Registration 51f101b441767ebddabdce2bd626553b

Access comprehensive regulatory information for “Abbott” SHBG 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 51f101b441767ebddabdce2bd626553b and manufactured by BIOKIT S.A.. 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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51f101b441767ebddabdce2bd626553b
Registration Details
Taiwan FDA Registration: 51f101b441767ebddabdce2bd626553b
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Device Details

“Abbott” SHBG Reagent Kit (Non-Sterile)
TW: “亞培”性荷爾蒙結合球蛋白檢驗試劑組(未滅菌)
Risk Class 1
MD

Registration Details

51f101b441767ebddabdce2bd626553b

Ministry of Health Medical Device Import No. 020085

DHA09402008506

Company Information

Product Details

Limited to the first level identification range of the "testicular lipoketone test system (A.1680)" of the Measures for the Administration of Medical Equipment.

A Clinical chemistry and clinical toxicology

A1680 Testicular Lipoketone Test System

Imported from abroad

Dates and Status

Jan 31, 2019

Jan 31, 2024