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"MP" Testosterone Test (Non-Sterile) - Taiwan Registration 8b44c228003a4ee3c2a210e8fb93a192

Access comprehensive regulatory information for "MP" Testosterone Test (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 8b44c228003a4ee3c2a210e8fb93a192 and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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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8b44c228003a4ee3c2a210e8fb93a192
Registration Details
Taiwan FDA Registration: 8b44c228003a4ee3c2a210e8fb93a192
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Device Details

"MP" Testosterone Test (Non-Sterile)
TW: "้ฆฌไธๅฝผๅพ—" ็ชไธธ่„‚้…ฎๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8b44c228003a4ee3c2a210e8fb93a192

Ministry of Health Medical Device Import No. 014349

DHA09401434902

Company Information

United States

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

Jul 21, 2014

Jul 21, 2024