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"Arno" single-lumen central venous catheter group - Taiwan Registration c57fef6b9bc276b0798a5291a2fbfc8f

Access comprehensive regulatory information for "Arno" single-lumen central venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c57fef6b9bc276b0798a5291a2fbfc8f and manufactured by Arrow International CR, a.s.;; Arrow International, Inc.(Subsidiary of Teleflex Inc.). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC(Subsidiary of Teleflex Incorporated), and 1 recent registrations in the same category. 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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c57fef6b9bc276b0798a5291a2fbfc8f
Registration Details
Taiwan FDA Registration: c57fef6b9bc276b0798a5291a2fbfc8f
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Device Details

"Arno" single-lumen central venous catheter group
TW: โ€œไบž่ซพโ€ๅ–ฎ่…”ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

c57fef6b9bc276b0798a5291a2fbfc8f

DHA05602692100

Company Information

Product Details

Details such as the validity of the Chinese imitation single approved version of the application is changed to: detailed as the approved Chinese instruction manual (the original approved label, instruction manual or packaging on January 16, 104 will be withdrawn and invalidated). The efficacy, use or indication is changed to: detailed as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on January 16, 104 shall be withdrawn and invalidated).

E Cardiovascular Medicine Science

E.1200 ่จบๆ–ท็”จ่ก€็ฎกๅ…งๅฐŽ็ฎก

import

Dates and Status

Dec 30, 2014

Dec 30, 2029

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