Taiwan FDA registration ab2c475ee2ba49f08dc05c9c2516651a
"Baiersev" Spirek cytoplasm separator tube sleeve
TW: “拜爾塞夫”思沛克血球細胞分離器管套組
Taiwan·Risk Class 2·BIOSAFE Ltd·Registered Feb 14, 2012 – Feb 14, 2027ActiveRegistration details
- Analysis ID
- ab2c475ee2ba49f08dc05c9c2516651a
- Customs Code
- DHA00602327602
Company information
- Manufacturer
- BIOSAFE Ltd
- Manufacturer Country
- Switzerland
- Authorized Representative
- COSMO MEDICAL SUPPLY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9100 Containers for the collection and disposal of blood and blood components
- Import Information
- import
Dates and status
- Registration Date
- Feb 14, 2012
- Expiry Date
- Feb 14, 2027
About this record
Access comprehensive regulatory information for "Baiersev" Spirek cytoplasm separator tube sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab2c475ee2ba49f08dc05c9c2516651a and manufactured by BIOSAFE Ltd. The authorized representative in Taiwan is COSMO MEDICAL SUPPLY CO., LTD..
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