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"Serenovas" remote guide tube - Taiwan Registration 8b46f1caa31f45d451f0d20711b38a37

Access comprehensive regulatory information for "Serenovas" remote 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 8b46f1caa31f45d451f0d20711b38a37 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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8b46f1caa31f45d451f0d20711b38a37
Registration Details
Taiwan FDA Registration: 8b46f1caa31f45d451f0d20711b38a37
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Device Details

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

Registration Details

8b46f1caa31f45d451f0d20711b38a37

DHA05602702401

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

Contract manufacturing;; input

Dates and Status

Feb 24, 2015

Feb 24, 2030