Taiwan FDA registration a850e7134dd2fd253a086255ff4f4a3d

"Vigut" micro blood collection system plasma test tubes

TW: "唯固特" 微量血液採集系統血漿試管

Taiwan·Risk Class 2·GREINER BIO-ONE GMBH·Registered Mar 02, 2006 – Mar 02, 2026Expired

Registration details

Analysis ID: a850e7134dd2fd253a086255ff4f4a3d
Customs Code: DHA00601607402

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 obtained from subcutaneous puncture of newborns, young children and critically ill patients.
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: Mar 02, 2006
Expiry Date: Mar 02, 2026

About this record

Access comprehensive regulatory information for "Vigut" micro blood collection system plasma test tubes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a850e7134dd2fd253a086255ff4f4a3d and manufactured by GREINER BIO-ONE GMBH. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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