Taiwan FDA registration 3c54bbc908845eb9483a782fc3dc150a
"Termao" Medi Safety Mini Lancet (Sterilized)
TW: 〝泰爾茂〞 美狄安全迷你採血針 (滅菌)
Registration details
- Analysis ID
- 3c54bbc908845eb9483a782fc3dc150a
- Customs Code
- DHA04401241104
Company information
- Manufacturer
- KOFU FACTORY OF TERUMO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 26, 2012
- Expiry Date
- Nov 26, 2027
About this record
Access comprehensive regulatory information for "Termao" Medi Safety Mini Lancet (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3c54bbc908845eb9483a782fc3dc150a and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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