Taiwan FDA registration d353e10c362584a12616b2e0807679ab
"Tienovi" torso equipment (unsterilized)
TW: "鐵諾威" 軀幹裝具 (未滅菌)
Taiwan·Risk Class 1·TECNOWAY S.R.L.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- d353e10c362584a12616b2e0807679ab
- Customs Code
- DHA08401940209
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 identification scope of the "Torso Equipment (O.3490)" classification and grading management measures for medical equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3490 Torso mounting
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Tienovi" torso 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 d353e10c362584a12616b2e0807679ab and manufactured by TECNOWAY S.R.L.. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING CO., LTD..
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