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"Lepu" hydrophilic guide wire - Taiwan Registration 61963c0f945b01f936508ca1bc725117

Access comprehensive regulatory information for "Lepu" hydrophilic guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61963c0f945b01f936508ca1bc725117 and manufactured by Lepu Medical (Europe) Cooperatief U.A.;; Lepu Medical Technology (Beijing) Co., Ltd.. The authorized representative in Taiwan is ApexMed Biomedical 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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61963c0f945b01f936508ca1bc725117
Registration Details
Taiwan FDA Registration: 61963c0f945b01f936508ca1bc725117
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Device Details

"Lepu" hydrophilic guide wire
TW: ใ€ๆจ‚ๆ™ฎใ€ž ่ฆชๆฐดๆ€งๅฐŽๅผ•ๅฐŽ็ทš
Risk Class 2

Registration Details

61963c0f945b01f936508ca1bc725117

DHA09200159608

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

Chinese goods;; input

Dates and Status

Sep 05, 2024

Sep 05, 2029