Taiwan FDA registration a63087ff0b99611553a64105e052a1a4
“Tokyo Iken” Super Lizer mini PRO Infrared therapy device
TW: “東京醫研” 超萊斯迷你專業版近紅外線治療儀
Taiwan·Risk Class 2·MD·TOKYO IKEN CO., LTD.·Registered Dec 27, 2021 – Dec 27, 2026ActiveRegistration details
- Analysis ID
- a63087ff0b99611553a64105e052a1a4
- License Form
- Ministry of Health Medical Device Import No. 035123
- Customs Code
- DHA05603512302
Company information
- Manufacturer
- TOKYO IKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- KROMAX INTERNATIONAL CORP.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5500 infrared light
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 27, 2021
- Expiry Date
- Dec 27, 2026
About this record
Access comprehensive regulatory information for “Tokyo Iken” Super Lizer mini PRO 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 a63087ff0b99611553a64105e052a1a4 and manufactured by TOKYO IKEN CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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