Accessory Kit for Manual Suction Pump 28 Fr; 40 Fr; 250 ml
Ref 30-56-000
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number42501056-1.8.3-WE 04250105628760 | Date23 Feb 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04250105628760 | Date4 May 2021 | StatusListed |
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- Withdrawn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
- United States
Specification
- Generic Name
- Emergency airway clearance suction system, manual
- Device Name
- Manual Suction Pump - Acc. Manual Suction Pump
- Model / Ref / Catalog
- 30-56-000
- Primary DI / UDI-DI
- 04250105628760
- Basic UDI-DI
- 42501056-1.8.3-WE
- FDA Product Code
- GCY
- EMDN Code
- R05010101 Respiratory suction probes without a control hole
- GMDN Term
- Emergency airway clearance suction system, manual
- Models / Variants
- Device Class
- Class I
- Regulation Number
- 878.4680
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- DE-MF-000005907
Other devices from VBM Medizintechnik GmbH
Properties
Other properties (19)
- 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
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No