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"Lanke Regent" Geimei guidewire - Taiwan Registration 71e7341e630a579e56d7ee4d3360ca13

Access comprehensive regulatory information for "Lanke Regent" Geimei guidewire in Taiwan's medical device market through Pure Global AI's free database. is registered under number 71e7341e630a579e56d7ee4d3360ca13 and manufactured by MANUFACTURED FOR ANGIODYNAMICS BY: LAKE REGION MANUFATURING CO. INC.. The authorized representative in Taiwan is PROMEDEX 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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71e7341e630a579e56d7ee4d3360ca13
Registration Details
Taiwan FDA Registration: 71e7341e630a579e56d7ee4d3360ca13
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Device Details

"Lanke Regent" Geimei guidewire
TW: "่—ๅ…‹้บ—ๆ™ถ" ๅ‰็พŽๅฐŽ็ตฒ
Cancelled

Registration Details

71e7341e630a579e56d7ee4d3360ca13

DHA00600980304

Company Information

Product Details

E Cardiovascular Medicine Science

import

Dates and Status

Jan 10, 2002

Jan 10, 2007

Nov 30, 2012

Cancellation Information

Logged out

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