Data / Medical devices / Denmark / Ward 24/7
Ward 24/7: FDA-registered device maker in Copenhagen K Hovedstaden, Denmark, 1 510(k) clearance
Ward 24/7 is registered with the FDA (registration 3036798186) in Copenhagen K Hovedstaden, Denmark. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 14, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036798186
- Address
- Danneskiold Samsoes Alle 41, Copenhagen K Hovedstaden, Denmark, 1434
- Owner or operator
- WARD 24/7 (10092852)
- Roles
- Manufacturer
- First device listed
- February 26, 2025
- Registered through
- 2026
- Brand names listed
- WARD247
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 14, 2025 | K241958 | WARD-CSS (v1.2.x) | MWI | Substantially Equivalent | Ward 24/7 Aps | accessdata.fda.gov |
Compare with other makers
Updated February 14, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.