Taiwan FDA registration 674b9f1796a8f579a03512ed8dfcc51e
"Abatec" xenon light source machine and accessories
TW: "阿巴鐵克"氙氣光源機及附件
Taiwan·Risk Class 2·APPLITEC LTD.·Registered Jul 17, 2006 – Jul 17, 2016CancelledRegistration details
- Analysis ID
- 674b9f1796a8f579a03512ed8dfcc51e
- Customs Code
- DHA00601688701
Company information
- Manufacturer
- APPLITEC LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Jul 17, 2006
- Expiry Date
- Jul 17, 2016
- Cancellation Date
- Nov 06, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Abatec" xenon light source machine and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 674b9f1796a8f579a03512ed8dfcc51e and manufactured by APPLITEC LTD.. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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