Taiwan FDA registration f8aa91eed6489c9c453b767a6abcacd4
"Baoya" plexus anesthesia needle
TW: “寶雅”神經叢麻醉針
Taiwan·Risk Class 2·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Mar 13, 2008 – Mar 13, 2013CancelledRegistration details
- Analysis ID
- f8aa91eed6489c9c453b767a6abcacd4
- Customs Code
- DHA00601872307
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- EVERMEDICAL COMPANY LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5140 Anesthesia transfer group
- Import Information
- import
Dates and status
- Registration Date
- Mar 13, 2008
- Expiry Date
- Mar 13, 2013
- Cancellation Date
- Jun 16, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baoya" plexus anesthesia needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8aa91eed6489c9c453b767a6abcacd4 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is EVERMEDICAL COMPANY LTD..
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