Taiwan FDA registration 498349d97369f8413fb835d0af07b92a
“BIOPTRON” LIGHT THERAPY SYSTEM
TW: “拜爾康”光療儀
Taiwan·Risk Class 2·MD·BIOPTRON AG·Registered Dec 05, 2016 – Dec 05, 2021CancelledRegistration details
- Analysis ID
- 498349d97369f8413fb835d0af07b92a
- License Form
- Ministry of Health Medical Device Import No. 029097
- Customs Code
- DHA05602909702
Company information
- Manufacturer
- BIOPTRON AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- Tianqun Medical Enterprise Co., Ltd
Product details
- 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
- Dec 05, 2016
- Expiry Date
- Dec 05, 2021
- Cancellation Date
- Jan 13, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “BIOPTRON” LIGHT THERAPY SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 498349d97369f8413fb835d0af07b92a and manufactured by BIOPTRON AG. The authorized representative in Taiwan is Tianqun Medical Enterprise Co., Ltd.
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