Taiwan FDA registration 77deb8cabfb800639691e30c49fef701
"Esker Rebien" Rui Laifei pulsed photometer
TW: “艾斯克雷比恩”芮萊膚脈衝光儀
Taiwan·Risk Class 2·ASCLEPION LASER TECHNOLOGIES GMBH·Registered Jan 24, 2011 – Jan 24, 2016CancelledRegistration details
- Analysis ID
- 77deb8cabfb800639691e30c49fef701
- Customs Code
- DHA00602191806
Company information
- Manufacturer
- ASCLEPION LASER TECHNOLOGIES GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Haotian Biotechnology 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
- Jan 24, 2011
- Expiry Date
- Jan 24, 2016
- Cancellation Date
- Feb 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 註銷藥商許可執照
About this record
Access comprehensive regulatory information for "Esker Rebien" Rui Laifei pulsed photometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77deb8cabfb800639691e30c49fef701 and manufactured by ASCLEPION LASER TECHNOLOGIES GMBH. The authorized representative in Taiwan is Haotian Biotechnology Co., Ltd.
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