Taiwan FDA registration 26e9916d096454cfdc59ef12eec1685b
"Lan" blood collection needle (sterile)
TW: "燁陞" 採血針 (滅菌)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Mar 15, 2016 – Mar 15, 2021CancelledRegistration details
- Analysis ID
- 26e9916d096454cfdc59ef12eec1685b
- Customs Code
- DHA09600266308
Company information
- Manufacturer Country
- China
- Authorized Representative
- YEHSHANG ENTERPRISE 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
- Input;; Chinese goods;; QMS/QSD
Dates and status
- Registration Date
- Mar 15, 2016
- Expiry Date
- Mar 15, 2021
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lan" blood collection needle (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 26e9916d096454cfdc59ef12eec1685b and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is YEHSHANG ENTERPRISE CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices