Single-use Laryngoscope Blade
by Shenzhen HugeMed Medical Technical Development Co., Ltd. 25 variants
Ref HS M4Model HS 2,HS 3,HS 4,HS M3,HS M4,HS P2,HS ML0
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 | Number69704625421057S 06970462542469 | Date8 Nov 2024 | 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- Withdrawn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
- Single-use Laryngoscope Blade
- Model / Reference
- HS 2, HS 3, HS 4, HS M3, HS M4, HS P2, HS ML0
- Primary DI / UDI-DI
- 06970462542469
- Basic UDI-DI
- 69704625421057S
- EMDN Code
- R9002 Laryngoscope blades, single-use
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000010895
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Shenzhen HugeMed Medical Technical Development Co., Ltd.
See all devices from Shenzhen HugeMed Medical Technical Development 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