Taiwan FDA registration d196815189fbe800f06683ce80c93248
"Nubis" Plinth (Non-sterile)
TW: "紐比斯"治療檯(未滅菌)
Taiwan·Risk Class 1·MD·AIRFUN D.O.O.·Registered May 27, 2019 – May 27, 2024CancelledRegistration details
- Analysis ID
- d196815189fbe800f06683ce80c93248
- License Form
- Ministry of Health Medical Device Import No. 020487
- Customs Code
- DHA09402048700
Company information
- Manufacturer
- AIRFUN D.O.O.
- Manufacturer Country
- Slovenia
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3520 treatment unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 27, 2019
- Expiry Date
- May 27, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Nubis" Plinth (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d196815189fbe800f06683ce80c93248 and manufactured by AIRFUN D.O.O.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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