Taiwan FDA registration ebc86a1a10f34526f819fb9e8bbc60c7
Rickres ophthalmic laser
TW: 雷克瑞斯眼科雷射
Taiwan·Risk Class 2·ELLEX MEDICAL PTY. LTD.·Registered Nov 22, 2007 – Nov 22, 2012CancelledRegistration details
- Analysis ID
- ebc86a1a10f34526f819fb9e8bbc60c7
- Customs Code
- DHA00601844900
Company information
- Manufacturer
- ELLEX MEDICAL PTY. LTD.
- Manufacturer Country
- Australia
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4392 後囊切除用Nd:YAG雷射
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2007
- Expiry Date
- Nov 22, 2012
- Cancellation Date
- Apr 16, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Rickres ophthalmic laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ebc86a1a10f34526f819fb9e8bbc60c7 and manufactured by ELLEX MEDICAL PTY. LTD.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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