Taiwan FDA registration 61963c0f945b01f936508ca1bc725117
"Lepu" hydrophilic guide wire
TW: 〝樂普〞 親水性導引導線
Taiwan·Risk Class 2·Lepu Medical (Europe) Cooperatief U.A.;; Lepu Medical Technology (Beijing) Co., Ltd.·Registered Sep 05, 2024 – Sep 05, 2029ActiveRegistration details
- Analysis ID
- 61963c0f945b01f936508ca1bc725117
- Customs Code
- DHA09200159608
Company information
- 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.1330 Catheter Guide Wires
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 05, 2024
- Expiry Date
- Sep 05, 2029
About this record
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..
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