Double Lumen Endobronchial Tube
by Royal Fornia Medical Equipment Co., Ltd. 10 variants
Ref QG-L-39FrModel QG-L-28Fr
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 | Number693801670003G2 06938016775831 | Date25 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- Withdrawn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
- QG-L-28Fr, QG-L-39Fr
- Primary DI / UDI-DI
- 06938016775831
- Basic UDI-DI
- 693801670003G2
- EMDN Code
- R01040202 Endobronchial oropharyngeal tubes, left
- Device Class
- Class IIa
- EU market of registration
- Romania
Manufacturer details
- EUDAMED SRN
- CN-MF-000008628
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Royal Fornia Medical Equipment Co., Ltd.
See all devices from Royal Fornia Medical Equipment 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