Taiwan FDA registration 8273d663721c1ac5a7db29b73cc8ccee

"Lepu" hydrophilic introducer set

TW: 〝樂普〞親水導引器套組

Taiwan·Risk Class 2·Lepu Medical (Europe) Cooperatief U.A.;; Lepu Medical Technology (Beijing) Co., Ltd.·Registered Nov 08, 2024 – Nov 08, 2029Active

Registration details

Analysis ID: 8273d663721c1ac5a7db29b73cc8ccee
Customs Code: DHA09200162808

Company information

Manufacturer: Lepu Medical (Europe) Cooperatief U.A.;; Lepu Medical Technology (Beijing) Co., Ltd.
Manufacturer Country: Netherlands;;China
Authorized Representative: ApexMed Biomedical Co., Ltd.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.1340 Catheter Introducers
Import Information: Input;; Chinese goods;; Contract manufacturing

Dates and status

Registration Date: Nov 08, 2024
Expiry Date: Nov 08, 2029

About this record

Access comprehensive regulatory information for "Lepu" hydrophilic introducer set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8273d663721c1ac5a7db29b73cc8ccee 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.