Taiwan FDA registration 406025c0887985469d748cc4f6f1f23f
"Pademk" ultrasound-guided nerve block therapy catheter group
TW: “帕將克”超音波導引神經阻斷治療導管組
Taiwan·Risk Class 2·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Sep 12, 2014 – Sep 12, 2029ActiveRegistration details
- Analysis ID
- 406025c0887985469d748cc4f6f1f23f
- Customs Code
- DHA05602655705
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 Anesthesiology
- Product Type (Level 2)
- D.5140 Anesthesia transfer group;; D.5120 Anesthesia delivery catheters;; D.5150 Anesthesia delivery puncture needle
- Import Information
- import
Dates and status
- Registration Date
- Sep 12, 2014
- Expiry Date
- Sep 12, 2029
About this record
Access comprehensive regulatory information for "Pademk" ultrasound-guided nerve block therapy catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 406025c0887985469d748cc4f6f1f23f and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices