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"Keithley" Ender Lilly implanted with fibrillation wires - Taiwan Registration eb25bd34c25a7cf828324427e63b5ab6

Access comprehensive regulatory information for "Keithley" Ender Lilly implanted with fibrillation wires in Taiwan's medical device market through Pure Global AI's free database. is registered under number eb25bd34c25a7cf828324427e63b5ab6 and manufactured by GUIDANT IRELAND. The authorized representative in Taiwan is Xiongqun Enterprise Limited.

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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eb25bd34c25a7cf828324427e63b5ab6
Registration Details
Taiwan FDA Registration: eb25bd34c25a7cf828324427e63b5ab6
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Device Details

"Keithley" Ender Lilly implanted with fibrillation wires
TW: "ๅ‰ๆ™‚ๅˆฉ" ๆฉๅพท็ฆฎไพ†ๅ…งๆค้™ค้กซๅฐŽ็ทš
Cancelled

Registration Details

eb25bd34c25a7cf828324427e63b5ab6

DHA00601007602

Company Information

Ireland

Product Details

vacuum

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

import

Dates and Status

Sep 12, 2002

Apr 21, 2010

Oct 26, 2012

Cancellation Information

Logged out

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