Taiwan FDA registration 793415790b4e41d18157b549e55f3ec0
"Bit seal" blood collection needle (sterilized)
TW: “位璽”採血針(滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jan 15, 2013 – Jan 15, 2018CancelledRegistration details
- Analysis ID
- 793415790b4e41d18157b549e55f3ec0
- Customs Code
- DHA04600182306
Company information
- Manufacturer Country
- China
- Authorized Representative
- Bit Seal 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
- Input;; Chinese goods;; QMS/QSD
Dates and status
- Registration Date
- Jan 15, 2013
- Expiry Date
- Jan 15, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bit seal" blood collection needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 793415790b4e41d18157b549e55f3ec0 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Bit Seal Biotechnology Co., Ltd.
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