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"Auswedish Kneput handheld carbon dioxide/oximeter - Taiwan Registration 22f851efa5ec30245eae9e9a3300d44e

Access comprehensive regulatory information for "Auswedish Kneput handheld carbon dioxide/oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22f851efa5ec30245eae9e9a3300d44e and manufactured by ORIDION MEDICAL 1987 LTD.;; COVIDIEN LLC. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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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22f851efa5ec30245eae9e9a3300d44e
Registration Details
Taiwan FDA Registration: 22f851efa5ec30245eae9e9a3300d44e
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Device Details

"Auswedish Kneput handheld carbon dioxide/oximeter
TW: โ€œๅฅง็‘žๅ…ธโ€ ่€ๆ™ฎ็‰นๆ‰‹ๆŒๅผไบŒๆฐงๅŒ–็ขณ/่ก€ๆฐงๆฟƒๅบฆ่จˆ
Risk Class 2
Cancelled

Registration Details

22f851efa5ec30245eae9e9a3300d44e

DHA05602787307

Company Information

Israel;;United States

Product Details

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

E Cardiovascular Medicine Science

E.2700.

Input;; Contract manufacturing

Dates and Status

Dec 11, 2015

Dec 11, 2020

Mar 16, 2017

Cancellation Information

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