Taiwan FDA registration 788c86ec4a7f6aa73e1f1fecc8d75088
Leishi Ophthalmic Erbium Chromium Laser
TW: 磊視眼科鉺雅鉻雷射儀
Taiwan·Risk Class 2·HOYA PHOTONICS, INC. D/B/A HOYA CONBIO;; ACE VISION GROUP·Registered Feb 23, 2011 – Feb 23, 2016CancelledRegistration details
- Analysis ID
- 788c86ec4a7f6aa73e1f1fecc8d75088
- Customs Code
- DHA00602217402
Company information
- Manufacturer Country
- United States
- Authorized Representative
- VISION RENU CORPORATION
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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Feb 23, 2011
- Expiry Date
- Feb 23, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Leishi Ophthalmic Erbium Chromium Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 788c86ec4a7f6aa73e1f1fecc8d75088 and manufactured by HOYA PHOTONICS, INC. D/B/A HOYA CONBIO;; ACE VISION GROUP. The authorized representative in Taiwan is VISION RENU CORPORATION.
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