Taiwan FDA registration 86a7ea0ec50bd8b67fc00c2375bbde86
TAG Heuer implant preloaded intraocular lens
TW: “豪雅”植入器預載式人工水晶體
Registration details
- Analysis ID
- 86a7ea0ec50bd8b67fc00c2375bbde86
- Customs Code
- DHA00602124902
Company information
- Manufacturer Country
- Singapore;;Japan
- Authorized Representative
- RAY HUNG INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Mar 06, 2012
- Expiry Date
- Jul 15, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for TAG Heuer implant preloaded intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 86a7ea0ec50bd8b67fc00c2375bbde86 and manufactured by HOYA MEDICAL SINGAPORE PTE LTD;; HOYA CORPORATION. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..
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