Taiwan FDA registration 8ca51ec2af1edf2aa6ffa4440bf670ff
"Termao" Medi Safety Mini Lancet (Unsterilized)
TW: 〝泰爾茂〞 美狄安全迷你採血筆 (未滅菌)
Registration details
- Analysis ID
- 8ca51ec2af1edf2aa6ffa4440bf670ff
- Customs Code
- DHA04401241002
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
- import
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 (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ca51ec2af1edf2aa6ffa4440bf670ff and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TAIDOC TECHNOLOGY 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