Vesscide
by Lepu Medical Technology (Beijing) Co., Ltd. 27 variants
Part of a family of 27 devices: see the family page
Ref 2.25 × 15
Vesscide (2.25 × 15) is a Class III device made by Lepu Medical Technology (Beijing) Co., Ltd., registered in EUDAMED on 11 Jun 2026 (Basic UDI-DI 69367337LP0046MW) with CE/MDR certificate MDR 818411 valid until 3 Aug 2030, active as of 25 Oct 2026.
Active
CE MDR
Valid until
3 Aug 2030
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69367337LP0046MW 06941785257057 | Date11 Jun 2026 | StatusActive |
Official records
- EUDAMED public site 69367337LP0046MW
Certificates
- MDR 818411 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 8 Apr 2026
- Expires
- 3 Aug 2030
- Reason
- Other
Timeline
- Certificate issued EUDAMED MDR 818411
- Registered EUDAMED 69367337LP0046MW
- Certificate expires EUDAMED MDR 818411
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Cutting Balloon Dilatation Catheter
- Model / reference
- 2.25 × 15
- Primary DI / UDI-DI
- 06941785257057
- Basic UDI-DI
- 69367337LP0046MW
- EMDN code
- C010401020101 Ptca balloon dilation catheters
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000001408
- Authorised representative
- Lepu Medical (Europe) Cooperatief U.A. NL-AR-000000551
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Other devices from Lepu Medical Technology (Beijing) Co., Ltd.
See all devices from Lepu Medical Technology (Beijing) Co., Ltd. →