Taiwan FDA registration 1331b0324168a228b94669c1f24f7c83
“KERA HARVEST” Diode Laser System
TW: “成果”二極體雷射系統
Taiwan·Risk Class 2·MD·KERA HARVEST INCORPORATION·Registered Nov 28, 2013 – Nov 28, 2023ExpiredRegistration details
- Analysis ID
- 1331b0324168a228b94669c1f24f7c83
- License Form
- Ministry of Health Medical Device Manufacturing No. 004238
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)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 28, 2013
- Expiry Date
- Nov 28, 2023
About this record
Access comprehensive regulatory information for “KERA HARVEST” Diode 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 1331b0324168a228b94669c1f24f7c83 and manufactured by KERA HARVEST INCORPORATION. The authorized representative in Taiwan is KERA HARVEST INCORPORATION.
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