Taiwan FDA registration ea17ac9b0992da57db69a844d0b29927
“DEKA” HIRO Nd YAG Laser Therapy Apparatus
TW: “德卡”喜樂雷射治療儀
Taiwan·Risk Class 2·MD·DEKA M.E.L.A. S.R.L.·Registered May 17, 2016 – May 17, 2026ExpiredRegistration details
- Analysis ID
- ea17ac9b0992da57db69a844d0b29927
- License Form
- Ministry of Health Medical Device Import No. 028537
- Customs Code
- DHA05602853709
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
- May 17, 2016
- Expiry Date
- May 17, 2026
About this record
Access comprehensive regulatory information for “DEKA” HIRO 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 ea17ac9b0992da57db69a844d0b29927 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is GAIA GENOMICS CORP..
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