Angiopower™
by Lepu Medical Technology (Beijing) Co., Ltd.
Ref LP-Z-30X, LP-P-40, LP-P-40SModel without logo on the device, with logo on the device
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69367337LP0025MN | Date22 Apr 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Inflation Device
- Model / Reference
- without logo on the device, LP-Z-30X, with logo on the device, LP-P-40, LP-P-40S
- Primary DI / UDI-DI
- 06941785252151, 06936733794128, 06936733794135
- Basic UDI-DI
- 69367337LP0025MN, 69367337LP0024ML
- EMDN Code
- C0104010280 Interventional coronary angiography devices - accessories
- Device Class
- Class I
- EU market of registration
- Lithuania
Manufacturer details
- EUDAMED SRN
- CN-MF-000001408
- Authorised representative
- Lepu Medical (Europe) Cooperatief U.A. NL-AR-000000551
Other devices from Lepu Medical Technology (Beijing) Co., Ltd.
See all devices from Lepu Medical Technology (Beijing) Co., Ltd. →
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No