Taiwan FDA registration b3df2db8418007e8e73c49f6d3f07725
"Sampe" ultrasonic spray therapy device
TW: "山普"超音波噴霧治療器
Taiwan·Risk Class 2·SAN UP S.A.·Registered Dec 11, 2006 – Dec 11, 2016CancelledRegistration details
- Analysis ID
- b3df2db8418007e8e73c49f6d3f07725
- Customs Code
- DHA00601748206
Company information
- Manufacturer
- SAN UP S.A.
- Manufacturer Country
- Argentina
- Authorized Representative
- Wellell Inc.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5630 Nebulizer
- Import Information
- import
Dates and status
- Registration Date
- Dec 11, 2006
- Expiry Date
- Dec 11, 2016
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sampe" ultrasonic spray therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b3df2db8418007e8e73c49f6d3f07725 and manufactured by SAN UP S.A.. The authorized representative in Taiwan is Wellell Inc..
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