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"Abbott" coronary artery envelope stent casting system - Taiwan Registration 55779b56f6a09469e980cce3a28f7c1a

Access comprehensive regulatory information for "Abbott" coronary artery envelope stent casting system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 55779b56f6a09469e980cce3a28f7c1a and manufactured by ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., 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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55779b56f6a09469e980cce3a28f7c1a
Registration Details
Taiwan FDA Registration: 55779b56f6a09469e980cce3a28f7c1a
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Device Details

"Abbott" coronary artery envelope stent casting system
TW: "ไบžๅŸน"ๅ† ็‹€ๅ‹•่„ˆๅŒ…่ฆ†ๆ”ฏๆžถๆšจๆ–ฝๆ”พ็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

55779b56f6a09469e980cce3a28f7c1a

DHA00601764304

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

Dec 29, 2006

Dec 29, 2016

Jun 26, 2018

Cancellation Information

Logged out

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