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"Febim" pressurized infusion machine (unsterilized) - Taiwan Registration 7cb05c6e56febe5c1a494172fc6f2db2

Access comprehensive regulatory information for "Febim" pressurized infusion machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7cb05c6e56febe5c1a494172fc6f2db2 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is NSH MEDICAL CORP..

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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7cb05c6e56febe5c1a494172fc6f2db2
Registration Details
Taiwan FDA Registration: 7cb05c6e56febe5c1a494172fc6f2db2
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Device Details

"Febim" pressurized infusion machine (unsterilized)
TW: โ€œ่ฒปๆฏ”ๅง†โ€ๅŠ ๅฃ“่ผธๆถฒๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7cb05c6e56febe5c1a494172fc6f2db2

DHA04400810508

Company Information

Germany

Product Details

Limited to the first level identification range of the classification and grading management method for medical equipment "Pressure apparatus for intravenous infusion bags (J.5420)".

J General hospital and personal use equipment

J.5420 ้œ่„ˆ่ผธๆถฒ่ข‹็”จๅฃ“ๅŠ›ๅ™จ

Input;; QMS/QSD

Dates and Status

Sep 16, 2009

Sep 16, 2029