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"Vigut" vacuum blood collection tube - serum test tube - Taiwan Registration 3fff257171267fa1f1fca84ae9aa8796

Access comprehensive regulatory information for "Vigut" vacuum blood collection tube - serum test tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fff257171267fa1f1fca84ae9aa8796 and manufactured by GREINER BIO-ONE GMBH. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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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3fff257171267fa1f1fca84ae9aa8796
Registration Details
Taiwan FDA Registration: 3fff257171267fa1f1fca84ae9aa8796
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Device Details

"Vigut" vacuum blood collection tube - serum test tube
TW: "ๅ”ฏๅ›บ็‰น" ็œŸ็ฉบ่ก€ๆถฒๆ”ถ้›†็ฎก-่ก€ๆธ…่ฉฆ็ฎก
Risk Class 2

Registration Details

3fff257171267fa1f1fca84ae9aa8796

DHA00601593902

Company Information

Austria

Product Details

Performance Change (Discretionary Performance Translation): Used to collect, transport, store and process blood for serotesting in clinical laboratories. The label and imitation order are changed to: as detailed as Chinese the approved copy of the imitation order (the original copy of the approved copy of the imitation label on July 02, 103 is withdrawn and invalidated). The following blanks.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

import

Dates and Status

Jan 24, 2006

Jan 24, 2026