Taiwan FDA registration cbe674c891c9edf27049888af79c050a
"Baxter" fuhemagglutination special application catheter
TW: “百特”伏血凝專用應用導管
Taiwan·Risk Class 3·BAXTER HEALTHCARE CORPORATION·Registered Apr 26, 2012 – Apr 26, 2027ActiveRegistration details
- Analysis ID
- cbe674c891c9edf27049888af79c050a
- Customs Code
- DHA00602355009
Company information
- Manufacturer
- BAXTER HEALTHCARE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4490 Absorbable hemostats and dressings
- Import Information
- import
Dates and status
- Registration Date
- Apr 26, 2012
- Expiry Date
- Apr 26, 2027
About this record
Access comprehensive regulatory information for "Baxter" fuhemagglutination special application catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cbe674c891c9edf27049888af79c050a and manufactured by BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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