Taiwan FDA registration c1b0b3f0c62f61f058f878f999f1324d
"Eye Care" ophthalmic excimer laser system
TW: “眼力健”眼科準分子雷射系統
Taiwan·Risk Class 3·AMO MANUFACTURING USA, LLC.·Registered Aug 18, 2009 – Aug 18, 2029ActiveRegistration details
- Analysis ID
- c1b0b3f0c62f61f058f878f999f1324d
- Customs Code
- DHA00602012301
Company information
- Manufacturer
- AMO MANUFACTURING USA, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
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.0001 眼科用準分子雷射系統
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2009
- Expiry Date
- Aug 18, 2029
About this record
Access comprehensive regulatory information for "Eye Care" ophthalmic excimer laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c1b0b3f0c62f61f058f878f999f1324d and manufactured by AMO MANUFACTURING USA, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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