Taiwan FDA registration cc7e25a109d81687a24914d5261136b3
"Aite" laser therapy instrument
TW: “艾特”雷射治療儀
Taiwan·Risk Class 2·ELTECH S.R.L·Registered Oct 03, 2012 – Oct 03, 2017CancelledRegistration details
- Analysis ID
- cc7e25a109d81687a24914d5261136b3
- Customs Code
- DHA00602398100
Company information
- Manufacturer
- ELTECH S.R.L
- Manufacturer Country
- Italy
- Authorized Representative
- MICROSTAR INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5500 Infrared lamp
- Import Information
- import
Dates and status
- Registration Date
- Oct 03, 2012
- Expiry Date
- Oct 03, 2017
- Cancellation Date
- Mar 18, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Aite" laser therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc7e25a109d81687a24914d5261136b3 and manufactured by ELTECH S.R.L. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS 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