Taiwan FDA registration 39a6b9bc884d88a32aed8e60d8f613e7
"Lianfa" Auto-Lancet Lancing Device (Non-sterile)
TW: "蓮發"採血筆(未滅菌)
Taiwan·Risk Class 1·MD·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Apr 22, 2014 – Apr 22, 2019CancelledRegistration details
- Analysis ID
- 39a6b9bc884d88a32aed8e60d8f613e7
- License Form
- Ministry of Health Medical Device Land Transport No. 002117
- Customs Code
- DHA09600211707
Company information
- Manufacturer Country
- China
- Authorized Representative
- YEHSHANG ENTERPRISE CORPORATION
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Apr 22, 2014
- Expiry Date
- Apr 22, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Lianfa" Auto-Lancet Lancing Device (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 39a6b9bc884d88a32aed8e60d8f613e7 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