Sekumatic Ndt
by Ecolab Deutschland GmbH 2 variants
Ref 3118430, 3111440, 3111460, 3111480, 3111390, 3118450
Active
CE MDD
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/MDD | NumberB-04028163118437 | Date1 Sep 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- Sekumatic Ndt - 10lSekumatic Ndt - 20lSekumatic Ndt - 200lSEKUMATIC NDT - 2x5L
- Model / Reference
- 3118430, 3111440, 3111460, 3111480, 3111390, 3118450
- Primary DI / UDI-DI
- 04028163118437, 04028163111445, 04028163111469, 04028163111483, 04028163111407, 04028163118451
- Basic UDI-DI
- B-04028163118437, B-04028163111445, B-04028163111469, B-04028163111483, B-04028163111407, B-04028163118451
- EMDN Code
- D0901 Ammonium salts for the disinfection of medical devices
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000004932
Other devices from Ecolab Deutschland GmbH
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No