Taiwan FDA registration 9fbf782d76d08b6e2959c33399c4b16e
“Iridex” Laser System
TW: “艾瑞斯” 眼科雷射系統
Taiwan·Risk Class 2·MD·IRIDEX CORPORATION.·Registered Mar 23, 2017 – Mar 23, 2027ActiveRegistration details
- Analysis ID
- 9fbf782d76d08b6e2959c33399c4b16e
- License Form
- Ministry of Health Medical Device Import No. 029422
- Customs Code
- DHA05602942200
Company information
- Manufacturer
- IRIDEX CORPORATION.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Mar 23, 2017
- Expiry Date
- Mar 23, 2027
About this record
Access comprehensive regulatory information for “Iridex” Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fbf782d76d08b6e2959c33399c4b16e and manufactured by IRIDEX CORPORATION.. The authorized representative in Taiwan is CLINICO INC..
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