Taiwan FDA registration bdd0cbb17fabde81d08089d7b3060a79
“DEKA” EXCILITE ULTRAVIOLET-THERAPY APPARATUS
TW: “德卡”紫外線治療器
Taiwan·Risk Class 2·MD·DEKA M.E.L.A. S.R.L.·Registered Jun 12, 2018 – Jun 12, 2028ActiveRegistration details
- Analysis ID
- bdd0cbb17fabde81d08089d7b3060a79
- License Form
- Ministry of Health Medical Device Import No. 031181
- Customs Code
- DHA05603118106
Company information
- Manufacturer
- DEKA M.E.L.A. S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- NEOASIA LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4630 UV lamp for dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 12, 2018
- Expiry Date
- Jun 12, 2028
About this record
Access comprehensive regulatory information for “DEKA” EXCILITE ULTRAVIOLET-THERAPY APPARATUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bdd0cbb17fabde81d08089d7b3060a79 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA 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