Taiwan FDA registration 23d0d7426dc39d6bbecf331f77ee3a39
Baxter applicator (unsterilized)
TW: “百特”塗藥器 (未滅菌)
Taiwan·Risk Class 1·BAXTER HEALTHCARE CORPORATION·Registered Jun 04, 2008 – Jun 04, 2018CancelledRegistration details
- Analysis ID
- 23d0d7426dc39d6bbecf331f77ee3a39
- Customs Code
- DHA04400678609
Company information
- Manufacturer
- BAXTER HEALTHCARE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Jun 04, 2008
- Expiry Date
- Jun 04, 2018
- Cancellation Date
- Nov 21, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Baxter applicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23d0d7426dc39d6bbecf331f77ee3a39 and manufactured by BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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