Taiwan FDA registration e5f8b5408838b7b0d33cb0b2b21f5bdf
“Optotek” Medical Therapeutic Laser Diode System
TW: “歐普特”二極體雷射治療系統
Taiwan·Risk Class 2·MD·OPTOTEK D.O.O.·Registered Nov 14, 2016 – Nov 14, 2021CancelledRegistration details
- Analysis ID
- e5f8b5408838b7b0d33cb0b2b21f5bdf
- License Form
- Ministry of Health Medical Device Import No. 029032
- Customs Code
- DHA05602903200
Company information
- Manufacturer
- OPTOTEK D.O.O.
- Manufacturer Country
- Slovenia
- Authorized Representative
- CLINICO INC.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4390 Ophthalmic laser unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2016
- Expiry Date
- Nov 14, 2021
- Cancellation Date
- Dec 03, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Optotek” Medical Therapeutic Laser Diode System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f8b5408838b7b0d33cb0b2b21f5bdf and manufactured by OPTOTEK D.O.O.. The authorized representative in Taiwan is CLINICO INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices