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Siliceous obstruction spherical duct - Taiwan Registration 5300a76d20e95eca11949347da4ecf47

Access comprehensive regulatory information for Siliceous obstruction spherical duct in Taiwan's medical device market through Pure Global AI's free database. is registered under number 5300a76d20e95eca11949347da4ecf47 and manufactured by AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION. The authorized representative in Taiwan is Swiss company Keith & Co., Ltd. Taipei 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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5300a76d20e95eca11949347da4ecf47
Registration Details
Taiwan FDA Registration: 5300a76d20e95eca11949347da4ecf47
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Device Details

Siliceous obstruction spherical duct
TW: ็Ÿฝ่ณช้˜ปๅกž็ƒๅฝขๅฐŽ็ฎก
Cancelled

Registration Details

5300a76d20e95eca11949347da4ecf47

DHA00600717402

Company Information

Product Details

0600 Intensive Care Unit and Cardiac Intensive Care Unit Equipment

Dates and Status

Apr 18, 1994

Apr 18, 1999

Aug 30, 2007

Cancellation Information

Logged out

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