"Serenovas" guide tube - Taiwan Registration e25837797dc6c8e4ebf5b70f7f5a0480
Access comprehensive regulatory information for "Serenovas" guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e25837797dc6c8e4ebf5b70f7f5a0480 and manufactured by Cerenovus, Inc.;; Medos International SARL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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e25837797dc6c8e4ebf5b70f7f5a0480
Registration Details
Taiwan FDA Registration: e25837797dc6c8e4ebf5b70f7f5a0480
Device Details
"Serenovas" guide tube
TW: โ่ณฝ็่ซพ่ฏๆฏโ ๅฐๅผๅฐ็ฎก
Risk Class 2

