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6F Codice hydrolytic thrombus removal duct - Taiwan Registration c294d16561be3df71971688a5c910c9e

Access comprehensive regulatory information for 6F Codice hydrolytic thrombus removal duct in Taiwan's medical device market through Pure Global AI's free database. is registered under number c294d16561be3df71971688a5c910c9e and manufactured by CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

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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c294d16561be3df71971688a5c910c9e
Registration Details
Taiwan FDA Registration: c294d16561be3df71971688a5c910c9e
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Device Details

6F Codice hydrolytic thrombus removal duct
TW: ๏ผ–๏ผฆใ€€่€ƒ่ฟชๆ–ฏๆฐด่งฃๅž‹่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก
Cancelled

Registration Details

c294d16561be3df71971688a5c910c9e

DHAS0600849002

Product Details

Vacuum.

0600 Intensive Care Unit and Cardiac Intensive Care Unit Equipment

import

Dates and Status

Dec 20, 1997

Dec 20, 2002

Jul 20, 2007

Cancellation Information

Logged out

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