Taiwan FDA registration 924054132144627a1f314a6455c52e9f
"Hermas" green laser system and its accessories
TW: “愛瑪士”綠光雷射系統及其配件
Taiwan·Risk Class 2·American Medical Systems, Innovation Center-Silicon Valley·Registered Mar 14, 2007 – Mar 14, 2017CancelledRegistration details
- Analysis ID
- 924054132144627a1f314a6455c52e9f
- Customs Code
- DHA00601781102
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
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
- Mar 14, 2007
- Expiry Date
- Mar 14, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Hermas" green laser system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 924054132144627a1f314a6455c52e9f and manufactured by American Medical Systems, Innovation Center-Silicon Valley. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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