Taiwan FDA registration e03f5fe0a3db4a976b685a28e0fd1c9f
"Hermaz" green laser system transmission device
TW: “愛瑪士”綠光雷射系統傳輸裝置
Taiwan·Risk Class 2·AMERICAN MEDICAL SYSTEMS INNOVATION CENTER-SILICON VALLEY·Registered Nov 15, 2007 – Nov 15, 2012CancelledRegistration details
- Analysis ID
- e03f5fe0a3db4a976b685a28e0fd1c9f
- Customs Code
- DHA00601844505
Company information
- Manufacturer Country
- United States
- Authorized Representative
- Conservation Corporation Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Nov 15, 2007
- Expiry Date
- Nov 15, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hermaz" green laser system transmission device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e03f5fe0a3db4a976b685a28e0fd1c9f and manufactured by AMERICAN MEDICAL SYSTEMS INNOVATION CENTER-SILICON VALLEY. The authorized representative in Taiwan is Conservation Corporation Limited.
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