"Philips" Zone Extreme/Select Support Catheter - Taiwan Registration 25d0ba5eccca7986a80ab8f5fe1b10df
Access comprehensive regulatory information for "Philips" Zone Extreme/Select Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25d0ba5eccca7986a80ab8f5fe1b10df and manufactured by Philips Image Guided Therapy Corporation. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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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25d0ba5eccca7986a80ab8f5fe1b10df
Registration Details
Taiwan FDA Registration: 25d0ba5eccca7986a80ab8f5fe1b10df
Device Details
"Philips" Zone Extreme/Select Support Catheter
TW: โ้ฃๅฉๆตฆโๅๅ
ๆฏๆฅต็ทป/้ธๆๆฏๆๅฐ็ฎก
Risk Class 2

