Laryngoscope Blade, Single Use
by Haymed Instruments 12 variants
Ref FMD-005-5020-02
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8964003352HM035F 08964003352592 | Date19 May 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- FMD-005-5020-02
- Primary DI / UDI-DI
- 08964003352592
- Basic UDI-DI
- 8964003352HM035F
- EMDN Code
- R9002 Laryngoscope blades, single-use
- Device Class
- Class I
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- PK-MF-000012992
- Authorised representative
- International Business Compendious of Sweden SE-AR-000001625
Other devices from Haymed Instruments
Properties
Other properties (13)
- Sterile: No
- 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