Taiwan FDA registration b250fea8281ae82ab76cb504518690c8
Continuous lancets (sterilized)
TW: 連發採血針(滅菌)
Taiwan·Risk Class 1·JINAN LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Mar 12, 2012 – Mar 12, 2017CancelledRegistration details
- Analysis ID
- b250fea8281ae82ab76cb504518690c8
- Customs Code
- DHA04600160407
Company information
- Manufacturer
- JINAN LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HMD BIOMEDICAL INC.
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;; QMS/QSD
Dates and status
- Registration Date
- Mar 12, 2012
- Expiry Date
- Mar 12, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Continuous lancets (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b250fea8281ae82ab76cb504518690c8 and manufactured by JINAN LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is HMD BIOMEDICAL INC..
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