Taiwan FDA registration dd399a686fd17d3d829a0b211e253067
"Tinović" limb equipment (unsterilized)
TW: "鐵諾威" 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·TECNOWAY S.R.L.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- dd399a686fd17d3d829a0b211e253067
- Customs Code
- DHA08401940301
Company information
- Manufacturer
- TECNOWAY S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Tinović" limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd399a686fd17d3d829a0b211e253067 and manufactured by TECNOWAY S.R.L.. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING CO., LTD..
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