Taiwan FDA registration 1018f26cc6ac948f721816032513886a
"Tranidium" 890 single wavelength phototherapy instrument
TW: "安絡定" 890單波長光療儀
Taiwan·Risk Class 2·ANODYNE THERAPY, LLC·Registered Mar 22, 2006 – Mar 22, 2021CancelledRegistration details
- Analysis ID
- 1018f26cc6ac948f721816032513886a
- Customs Code
- DHA00601418205
Company information
- Manufacturer
- ANODYNE THERAPY, LLC
- Manufacturer Country
- United States
- Authorized Representative
- HOLY STONE HEALTHCARE CO., LTD.
Product details
- Intended Use
- Improves blood circulation, relieves muscle fatigue and stiffness.
- Product Type (Level 1)
- o Physical Medical Sciences
- Import Information
- import
Dates and status
- Registration Date
- Mar 22, 2006
- Expiry Date
- Mar 22, 2021
- Cancellation Date
- Aug 04, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Tranidium" 890 single wavelength phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1018f26cc6ac948f721816032513886a and manufactured by ANODYNE THERAPY, LLC. The authorized representative in Taiwan is HOLY STONE HEALTHCARE CO., LTD..
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