Interventional Drape
by Leboo (Hubei) Healthcare Products Limited
Ref Interventional DrapeModel Interventional Drape、Pacemaker Drape with Single Aperture、Pacemaker Drape with Dual Apertures
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 | Number697519784Z83X5 06975197849531 | Date16 Sep 2025 | 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- Withdrawn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
- Model / Reference
- Interventional Drape、Pacemaker Drape with Single Aperture、Pacemaker Drape with Dual Apertures, Interventional Drape
- Primary DI / UDI-DI
- 06975197849531
- Basic UDI-DI
- 697519784Z83X5
- EMDN Code
- T020102 Specialistic surgery drapes
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000021186
- Authorised representative
- Share info GmbH DE-AR-000005132
Other devices from Leboo (Hubei) Healthcare Products Limited
See all devices from Leboo (Hubei) Healthcare Products Limited →
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