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"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
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Device Details

"Serenovas" guide tube
TW: โ€œ่ณฝ็‘ž่ซพ่ฏๆ–ฏโ€ ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2

Registration Details

e25837797dc6c8e4ebf5b70f7f5a0480

DHA05602543703

Company Information

Mexico;;Switzerland

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Oct 18, 2013

Oct 18, 2028