Taiwan FDA registration 22d7bc5b28c345fbb44cbb11c3a47650
“PAJUNK” Sono System for Ultrasound Guided Nerve Blocks
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 May 02, 2014 – May 02, 2024ExpiredRegistration details
- Analysis ID
- 22d7bc5b28c345fbb44cbb11c3a47650
- License Form
- Ministry of Health Medical Device Import No. 026132
- Customs Code
- DHA05602613202
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- Stimulation and ultrasound techniques are used to achieve the effect of continuous peripheral nerve block anesthesia
- 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
- May 02, 2014
- Expiry Date
- May 02, 2024
About this record
Access comprehensive regulatory information for “PAJUNK” Sono System for Ultrasound Guided Nerve Blocks in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22d7bc5b28c345fbb44cbb11c3a47650 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
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