Taiwan FDA registration 261b23eba7f96397642cacaea056bc77
"Puang" Sharp Peripheral Blood Needle (Sterilization)
TW: "普昂" 暢銳 末梢採血針 (滅菌)
Taiwan·Risk Class 1·PROMISEMED HANGZHOU MEDITECH CO., LTD.·Registered Mar 19, 2024 – Mar 19, 2029ActiveRegistration details
- Analysis ID
- 261b23eba7f96397642cacaea056bc77
- Customs Code
- DHA09600490605
Company information
- Manufacturer
- PROMISEMED HANGZHOU MEDITECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- 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;; QMS/QSD;; input
Dates and status
- Registration Date
- Mar 19, 2024
- Expiry Date
- Mar 19, 2029
About this record
Access comprehensive regulatory information for "Puang" Sharp Peripheral Blood Needle (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 261b23eba7f96397642cacaea056bc77 and manufactured by PROMISEMED HANGZHOU MEDITECH CO., LTD.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL 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