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"Serenovas" Emberway suction catheter - Taiwan Registration b070233308d0c3171ada83cb4328c1c6

Access comprehensive regulatory information for "Serenovas" Emberway suction catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b070233308d0c3171ada83cb4328c1c6 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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b070233308d0c3171ada83cb4328c1c6
Registration Details
Taiwan FDA Registration: b070233308d0c3171ada83cb4328c1c6
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Device Details

"Serenovas" Emberway suction catheter
TW: โ€œ่ณฝ็‘ž่ซพ่ฏๆ–ฏโ€ๆฉๆŸๅ”ฏๆŠฝๅธๅฐŽ็ฎก
Risk Class 2

Registration Details

b070233308d0c3171ada83cb4328c1c6

DHA05603421601

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

Input;; Contract manufacturing

Dates and Status

Dec 11, 2020

Dec 11, 2025