Taiwan FDA registration f4499e33cbe8b78a69d8aeb7f8855b21
Wuding Anshinken II blood collector (unsterilized)
TW: 五鼎安伸軒II採血器 (未滅菌)
Registration details
- Analysis ID
- f4499e33cbe8b78a69d8aeb7f8855b21
- Customs Code
- DHA04400903801
Company information
- Manufacturer Country
- United States
- Authorized Representative
- APEX BIOTECHNOLOGY CORPORATION
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
- Aug 04, 2010
- Expiry Date
- Aug 04, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Wuding Anshinken II blood collector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4499e33cbe8b78a69d8aeb7f8855b21 and manufactured by BAYER HEALTHCARE LLC, A SUBSIDIARY OF BAYER CORPORATION, DIABETES CARE. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.
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