Taiwan FDA registration a34f4aa6552019df95f82de6d985affc
"Translite" Transilluminator (Non-Sterile)
TW: "穿視來透"透照器(未滅菌)
Taiwan·Risk Class 1·MD·TRANSLITE LLC·Registered Dec 11, 2015 – Dec 11, 2020CancelledRegistration details
- Analysis ID
- a34f4aa6552019df95f82de6d985affc
- License Form
- Ministry of Health Medical Device Import No. 015964
- Customs Code
- DHA09401596401
Company information
- Manufacturer
- TRANSLITE LLC
- Manufacturer Country
- United States
- Authorized Representative
- ADENT MED CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1945 transillumination
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 11, 2015
- Expiry Date
- Dec 11, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Translite" Transilluminator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a34f4aa6552019df95f82de6d985affc and manufactured by TRANSLITE LLC. The authorized representative in Taiwan is ADENT MED CO., LTD..
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