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"Abbot" Marklin coronary artery dilation catheter - Taiwan Registration 3f9924792744f3b533ea827bcbd0df35

Access comprehensive regulatory information for "Abbot" Marklin coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3f9924792744f3b533ea827bcbd0df35 and manufactured by ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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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3f9924792744f3b533ea827bcbd0df35
Registration Details
Taiwan FDA Registration: 3f9924792744f3b533ea827bcbd0df35
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Device Details

"Abbot" Marklin coronary artery dilation catheter
TW: โ€œไบžๅŸนโ€้ฆฌๅ…‹ๆž—ๅ† ็‹€ๅ‹•่„ˆๆ“ดๅผตๅฐŽ็ฎก
Risk Class 3
Cancelled

Registration Details

3f9924792744f3b533ea827bcbd0df35

DHA00601885409

Product Details

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

E Cardiovascular Medicine Science

E.0005.

import

Dates and Status

May 12, 2008

May 12, 2013

Sep 26, 2016

Cancellation Information

Logged out

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