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"Pademk" ultrasound-guided nerve block therapy catheter group - Taiwan Registration 406025c0887985469d748cc4f6f1f23f

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.

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406025c0887985469d748cc4f6f1f23f
Registration Details
Taiwan FDA Registration: 406025c0887985469d748cc4f6f1f23f
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Device Details

"Pademk" ultrasound-guided nerve block therapy catheter group
TW: โ€œๅธ•ๅฐ‡ๅ…‹โ€่ถ…้ŸณๆณขๅฐŽๅผ•็ฅž็ถ“้˜ปๆ–ทๆฒป็™‚ๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

406025c0887985469d748cc4f6f1f23f

DHA05602655705

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5140 Anesthesia transfer group;; D.5120 Anesthesia delivery catheters;; D.5150 Anesthesia delivery puncture needle

import

Dates and Status

Sep 12, 2014

Sep 12, 2029