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"MP" Progesterone Test (Non-Sterile) - Taiwan Registration 0cfff06b18188e926e1733d81d3e84c5

Access comprehensive regulatory information for "MP" Progesterone 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 0cfff06b18188e926e1733d81d3e84c5 and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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0cfff06b18188e926e1733d81d3e84c5
Registration Details
Taiwan FDA Registration: 0cfff06b18188e926e1733d81d3e84c5
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Device Details

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

Registration Details

0cfff06b18188e926e1733d81d3e84c5

Ministry of Health Medical Device Import No. 014348

DHA09401434800

Company Information

United States

Product Details

Limited to the first level identification range of the "Progesterone Test System (A.1620)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1620 Progesterone Test System

Imported from abroad

Dates and Status

Jul 21, 2014

Jul 21, 2024