Taiwan FDA registration ab6953e91bcac9b356d7921ad9d21062
“PAJUNK” SonoPlex Stim Cannula
TW: “帕將克”超音波導引神經阻斷導管組
Taiwan·Risk Class 2·MD·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Oct 23, 2013 – Oct 23, 2028ActiveRegistration details
- Analysis ID
- ab6953e91bcac9b356d7921ad9d21062
- License Form
- Ministry of Health Medical Device Import No. 025441
- Customs Code
- DHA05602544107
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5140 Anesthesia Transport Group
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 23, 2013
- Expiry Date
- Oct 23, 2028
About this record
Access comprehensive regulatory information for “PAJUNK” SonoPlex Stim Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab6953e91bcac9b356d7921ad9d21062 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
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