Taiwan FDA registration 19985321ab1e4d3b377fca7346efc0de
"Results" excimer laser system
TW: “成果”準分子雷射系統
Registration details
- Analysis ID
- 19985321ab1e4d3b377fca7346efc0de
Company information
- Manufacturer
- KERA HARVEST INCORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KERA HARVEST INCORPORATION
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
- Domestic
Dates and status
- Registration Date
- May 09, 2012
- Expiry Date
- May 09, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Results" 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 19985321ab1e4d3b377fca7346efc0de and manufactured by KERA HARVEST INCORPORATION. The authorized representative in Taiwan is KERA HARVEST INCORPORATION.
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