Double Lumen Endobronchial Tube
by Ningbo Luke Medical Devices Co., LTD 14 variants
Ref EBT35L(DLT35L)Model Double Lumen Endobronchial Tube
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 | Number697024089EBTPA 06970240890386 | Date20 May 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- Withdrawn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
- Double Lumen Endobronchial Tube
- Model / Reference
- Double Lumen Endobronchial Tube, EBT35L(DLT35L)
- Primary DI / UDI-DI
- 06970240890386
- Basic UDI-DI
- 697024089EBTPA
- Direct Marketing DI
- 06970240890386
- EMDN Code
- R01040202 Endobronchial oropharyngeal tubes, left
- Device Class
- Class IIa
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- CN-MF-000011732
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Ningbo Luke Medical Devices 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