Taiwan FDA registration b096ccef28192064c5e425d122f6950c
“Tokyo Iken” Super Lizer Near-Infrared therapy device
TW: “東京醫研”近紅外線治療儀
Taiwan·Risk Class 2·MD·TOKYO IKEN CO., LTD.·Registered Aug 10, 2018 – Aug 10, 2028ActiveRegistration details
- Analysis ID
- b096ccef28192064c5e425d122f6950c
- License Form
- Ministry of Health Medical Device Import No. 031240
- Customs Code
- DHA05603124009
Company information
- Manufacturer
- TOKYO IKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- KROMAX INTERNATIONAL 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 10, 2018
- Expiry Date
- Aug 10, 2028
About this record
Access comprehensive regulatory information for “Tokyo Iken” Super Lizer Near-Infrared 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 b096ccef28192064c5e425d122f6950c and manufactured by TOKYO IKEN CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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