"Vigut" microblood collection system - ethylenediaminetetraacetic acid test tube
Taiwan·Risk Class 2·GREINER BIO-ONE GMBH·Registered Jan 24, 2006 – Jan 24, 2016Cancelled- Analysis ID
- 92310164b5d8d6d2942b18b01c8097e7
- Customs Code
- DHA00601594102
- Manufacturer
- GREINER BIO-ONE GMBH
- Manufacturer Country
- Austria
- Authorized Representative
- SCN TRADING COMPANY LIMITED
- 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
- Registration Date
- Jan 24, 2006
- Expiry Date
- Jan 24, 2016
- Cancellation Date
- May 17, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Vigut" microblood collection system - ethylenediaminetetraacetic acid 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 92310164b5d8d6d2942b18b01c8097e7 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, 1 companies making similar products including GREINER BIO-ONE GMBH, and 1 recent registrations in the same category. 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.