Taiwan FDA registration dfaeb23a55f84679cb902dd2c0cd157e
"Newbis" treatment table (unsterilized)
TW: "紐比斯"治療檯(未滅菌)
Taiwan·Risk Class 1·AIRFUN D.O.O.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- dfaeb23a55f84679cb902dd2c0cd157e
- Customs Code
- DHA08402048704
Company information
- Manufacturer
- AIRFUN D.O.O.
- Manufacturer Country
- Slovenia
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Treatment Table (O.3520)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3520 Therapeutic cage
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Newbis" treatment table (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfaeb23a55f84679cb902dd2c0cd157e and manufactured by AIRFUN D.O.O.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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