Taiwan FDA registration 6ffaac7c411e1b4a5626d93a506bab1f
“DEKA” SH1 Nd YAG Laser Therapy Apparatus
TW: “德卡”喜望雷射治療儀
Taiwan·Risk Class 2·MD·DEKA M.E.L.A. S.R.L.·Registered Aug 31, 2017 – Aug 31, 2027ActiveRegistration details
- Analysis ID
- 6ffaac7c411e1b4a5626d93a506bab1f
- License Form
- Ministry of Health Medical Device Import No. 030168
- Customs Code
- DHA05603016809
Company information
- Manufacturer
- DEKA M.E.L.A. S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- GAIA GENOMICS CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5500 infrared light
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 31, 2017
- Expiry Date
- Aug 31, 2027
About this record
Access comprehensive regulatory information for “DEKA” SH1 Nd YAG Laser 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 6ffaac7c411e1b4a5626d93a506bab1f and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is GAIA GENOMICS CORP..
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