Taiwan FDA registration 61fb3b23afd20f1866f4b5f1c4400836
"Age" automatic needle withdrawal pen (unsterilized)
TW: 〝暐世〞自動退針採血筆 (未滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Dec 20, 2011 – Dec 20, 2021CancelledRegistration details
- Analysis ID
- 61fb3b23afd20f1866f4b5f1c4400836
- Customs Code
- DHA04600154300
Company information
- Manufacturer Country
- China
- Authorized Representative
- Hsinchu General Factory of Weishi Biotechnology Co., 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
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 20, 2011
- Expiry Date
- Dec 20, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Age" automatic needle withdrawal pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 61fb3b23afd20f1866f4b5f1c4400836 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Hsinchu General Factory of Weishi Biotechnology Co., Ltd.
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