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"Fertipro" SpermMar (Non-Sterile) - Taiwan Registration d3092e846ad84b486cbd014e89a5af67

Access comprehensive regulatory information for "Fertipro" SpermMar (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 d3092e846ad84b486cbd014e89a5af67 and manufactured by FERTIPRO N.V.. The authorized representative in Taiwan is ESSENCE EQUIP CO., LTD..

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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d3092e846ad84b486cbd014e89a5af67
Registration Details
Taiwan FDA Registration: d3092e846ad84b486cbd014e89a5af67
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Device Details

"Fertipro" SpermMar (Non-Sterile)
TW: "่ฒปๆๆ™ฎ็พ…" ็ฒพ่Ÿฒๅ…็–ซๆŠ—้ซ”ๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d3092e846ad84b486cbd014e89a5af67

Ministry of Health Medical Device Import No. 016336

DHA09401633603

Company Information

Belgium

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Human Whole Plasma or Serum Immunoassay System (C.5700)".

C Immunology and microbiology devices

C5700 Human whole plasma or serum immunoassay system

Imported from abroad

Dates and Status

Mar 30, 2016

Mar 30, 2026