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“Smiths” Portex Tracheostomy Tube - Taiwan Registration 16bd219539173459e4ab00e352b89d26

Access comprehensive regulatory information for “Smiths” Portex Tracheostomy Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16bd219539173459e4ab00e352b89d26 and manufactured by Smiths Medical Czech Republic a.s.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

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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16bd219539173459e4ab00e352b89d26
Registration Details
Taiwan FDA Registration: 16bd219539173459e4ab00e352b89d26
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Device Details

“Smiths” Portex Tracheostomy Tube
TW: “史密斯”保德士氣切套管
Risk Class 2
MD

Registration Details

16bd219539173459e4ab00e352b89d26

Ministry of Health Medical Device Import No. 030167

DHA05603016707

Company Information

Product Details

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

D Devices for anesthesiology

D5800 Trachetomy tube and its balloon

Imported from abroad

Dates and Status

Aug 31, 2017

Aug 31, 2027