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"Ceranowas" Pauler Extended Microtube - Taiwan Registration 4b58a5bbe748ffd0451f591666edd9b1

Access comprehensive regulatory information for "Ceranowas" Pauler Extended Microtube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b58a5bbe748ffd0451f591666edd9b1 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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4b58a5bbe748ffd0451f591666edd9b1
Registration Details
Taiwan FDA Registration: 4b58a5bbe748ffd0451f591666edd9b1
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Device Details

"Ceranowas" Pauler Extended Microtube
TW: โ€œ่ณฝ็‘ž่ซพ่ฏๆ–ฏโ€ ไฟๅ‹’ๅŠ ้•ทๅž‹ๅพฎๅฐŽ็ฎก
Risk Class 2

Registration Details

4b58a5bbe748ffd0451f591666edd9b1

DHA05603724102

Company Information

Mexico;;Switzerland

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1210.

Contract manufacturing;; input

Dates and Status

Jul 08, 2024

Jul 08, 2029