Taiwan FDA registration bbcf6c6e2c39a5c1e5c764cc3a7ffe3f
"Vigut" vacuum blood collection tube - heparin test tube
TW: "唯固特" 真空血液收集管-肝素試管
Taiwan·Risk Class 2·GREINER BIO-ONE GMBH·Registered Jan 23, 2006 – Jan 23, 2026ExpiredRegistration details
- Analysis ID
- bbcf6c6e2c39a5c1e5c764cc3a7ffe3f
- Customs Code
- DHA00601592800
Company information
- Manufacturer
- GREINER BIO-ONE GMBH
- Manufacturer Country
- Austria
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- It is used to collect, transport and process blood for plasma or whole blood testing in clinical laboratories.
- 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 23, 2006
- Expiry Date
- Jan 23, 2026
About this record
Access comprehensive regulatory information for "Vigut" vacuum blood collection tube - heparin 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 bbcf6c6e2c39a5c1e5c764cc3a7ffe3f and manufactured by GREINER BIO-ONE GMBH. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
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