Taiwan FDA registration 70331f7a9b9155d81b20f64ead95b683
Baxter arteriovenous needles
TW: 百特動靜脈廔管針
Taiwan·Risk Class 2·NIPRO (THAILAND) CORPORATION LIMITED·Registered Sep 14, 2007 – Sep 14, 2022CancelledRegistration details
- Analysis ID
- 70331f7a9b9155d81b20f64ead95b683
- Customs Code
- DHA00601832600
Company information
- Manufacturer
- NIPRO (THAILAND) CORPORATION LIMITED
- Manufacturer Country
- Thailand
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5540 Blood Access Devices and Accessories
- Import Information
- import
Dates and status
- Registration Date
- Sep 14, 2007
- Expiry Date
- Sep 14, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Baxter arteriovenous needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 70331f7a9b9155d81b20f64ead95b683 and manufactured by NIPRO (THAILAND) CORPORATION LIMITED. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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