Taiwan FDA registration 765989e7c2fa0ecd7142fe3b08145c59
"Emma" excimer therapy device
TW: “艾瑪”準分子治療儀
Taiwan·Risk Class 2·Alma Lasers GmbH;; Alma Lasers Ltd.·Registered Nov 07, 2017 – Nov 07, 2022CancelledRegistration details
- Analysis ID
- 765989e7c2fa0ecd7142fe3b08145c59
- Customs Code
- DHA05603038201
Company information
- Manufacturer
- Alma Lasers GmbH;; Alma Lasers Ltd.
- Manufacturer Country
- Israel;;Germany
- Authorized Representative
- GAIA GENOMICS CORP.
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.4630 皮膚病用紫外線燈
- Import Information
- import
Dates and status
- Registration Date
- Nov 07, 2017
- Expiry Date
- Nov 07, 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 "Emma" excimer therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 765989e7c2fa0ecd7142fe3b08145c59 and manufactured by Alma Lasers GmbH;; Alma Lasers Ltd.. The authorized representative in Taiwan is GAIA GENOMICS CORP..
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