Taiwan FDA registration 3fff257171267fa1f1fca84ae9aa8796

"Vigut" vacuum blood collection tube - serum test tube

TW: "唯固特" 真空血液收集管-血清試管
Taiwan flagTaiwan·Risk Class 2·GREINER BIO-ONE GMBH·Registered Jan 24, 2006 – Jan 24, 2026Expired
Registration details
Analysis ID
3fff257171267fa1f1fca84ae9aa8796
Customs Code
DHA00601593902
Company information
Manufacturer Country
Austria
Authorized Representative
SCN TRADING COMPANY LIMITED
Product details
Intended Use
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approved copy of the imitation order (the original copy of the approved copy of the imitation label on July 02, 103 is withdrawn and invalidated).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.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1675 Blood collection equipment
Import Information
import
Dates and status
Registration Date
Jan 24, 2006
Expiry Date
Jan 24, 2026
About this record

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.

Free DatabasePowered by Pure Global AI89,000+ Devices