Taiwan FDA registration 16299176cfb138fabd3eca37918ecbe1
“Rexxam” Ophthalmic Trial Lens Set (Non-Sterile)
TW: “隆祥” 眼科試驗鏡片組 (未滅菌)
Taiwan·Risk Class 1·MD·REXXAM CO., LTD. KAGAWA FACTORY·Registered Feb 02, 2021 – Feb 02, 2026ExpiredRegistration details
- Analysis ID
- 16299176cfb138fabd3eca37918ecbe1
- License Form
- Ministry of Health Medical Device Import No. 022287
- Customs Code
- DHA09402228702
Company information
- Manufacturer
- REXXAM CO., LTD. KAGAWA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1405 Ophthalmic Test Lens Group
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 02, 2021
- Expiry Date
- Feb 02, 2026
About this record
Access comprehensive regulatory information for “Rexxam” Ophthalmic Trial Lens Set (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 16299176cfb138fabd3eca37918ecbe1 and manufactured by REXXAM CO., LTD. KAGAWA FACTORY. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..
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