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Sign in to claim this brandRAULAND-BORG CORPORATION
US
Last updated September 17, 2026
What RAULAND-BORG CORPORATION makes
Rauland-Borg Corporation manufactures nurse call systems, specifically the Responder product line.
These devices are classified as Class I medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- 1802 West Central Road, Mount Prospect, IL, 60056
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000227151
- DUNS Number
- —
Catalogue (170)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Responder | 352004 | FDA UDI | Class I | Active |
| Responder | 353010 | FDA UDI | Class I | Active |
| Responder | R5KCL506 | FDA UDI | Class I | Unknown |
| Responder | R5KDC46 | FDA UDI | Class I | Unknown |
| Responder | R5KPS1A | FDA UDI | Class I | Unknown |
| Responder | R4K22A | FDA UDI | Class I | Unknown |
| Responder | R5KMPR36 | FDA UDI | Class I | Active |
| Responder | 354026 | FDA UDI | Class I | Active |
| Responder | 3225300 | FDA UDI | Class I | Unknown |
| Responder | R5KUPB2 | FDA UDI | Class I | Unknown |
| Responder | R4K15V | FDA UDI | Class I | Active |
| Responder | R5KDC06V2 | FDA UDI | Class I | Active |
| Responder | NCLCD | FDA UDI | Class I | Unknown |
| Responder | R4KANNV2 | FDA UDI | Class I | Active |
| Responder | R5KSMSTV2 | FDA UDI | Class I | Active |
| Responder | 352021 | FDA UDI | Class I | Unknown |
| Responder | NCDUTY | FDA UDI | Class I | Unknown |
| Responder | R5KPD2A | FDA UDI | Class I | Unknown |
| Responder | R4K12A | FDA UDI | Class I | Unknown |
| Responder | 354011 | FDA UDI | Class I | Unknown |
| Responder | 350034 | FDA UDI | Class I | Unknown |
| Responder | 354001WP | FDA UDI | Class I | Active |
| Responder | 354027 | FDA UDI | Class I | Active |
| Responder | R5KCANCELV2 | FDA UDI | Class I | Active |
| Responder | R5KSDTYV2 | FDA UDI | Class I | Active |
| Responder | DCA200 | FDA UDI | Class I | Unknown |
| Responder | R5KAUDPCV2 | FDA UDI | Class I | Active |
| Responder | 352010 | FDA UDI | Class I | Unknown |
| Responder | R5KDC46V2 | FDA UDI | Class I | Active |
| Responder | 350300 | FDA UDI | Class I | Active |
| Responder | NCPBPH | FDA UDI | Class I | Unknown |
| Responder | 301103 | FDA UDI | Class I | Unknown |
| Responder | R5KCL546V2 | FDA UDI | Class I | Active |
| Responder | R5KSSTFV2 | FDA UDI | Class I | Active |
| Responder | R5KMPR36GSA | FDA UDI | Class I | Active |
| Responder | CLA246 | FDA UDI | Class I | Active |
| Responder | DCV116 | FDA UDI | Class I | Unknown |
| Responder | 354021 | FDA UDI | Class I | Active |
| Responder | R5KCONS | FDA UDI | Class I | Unknown |
| Responder | NCNSCB | FDA UDI | Class I | Unknown |
| Responder | 351004 | FDA UDI | Class I | Active |
| Responder | R5KPS1LCAV2 | FDA UDI | Class I | Active |
| Responder | HSS401 | FDA UDI | Class I | Active |
| Responder | NCLED6 | FDA UDI | Class I | Unknown |
| Responder | 351008 | FDA UDI | Class I | Active |
| Responder | R4KSAR | FDA UDI | Class I | Active |
| Responder | 351311 | FDA UDI | Class I | Active |
| Responder | R4KCB12 | FDA UDI | Class I | Unknown |
| Responder | R5KMSCV2 | FDA UDI | Class I | Active |
| Responder | 351300 | FDA UDI | Class I | Unknown |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Rauland-Borg Corporation has one FDA recall record, initiated on 2013-05-10, with a status listed as terminated. The recall reason states that a counterfeited electronic component, specifically a data transceiver used for intercommunication in the Responder 5 system on the L-Net data path, was identified in the affected products.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 10, 2013 | Z-2213-2013 | — | terminated | A counterfeited electronic component was identified in the products affected. The component, a data transceiver (transmitter/receiver), is associated with the intercommunication of these devices in the Responder 5 system across the L-Net data path. Failure of a data transceiver results in the loss of nurse call functionality in the associated room, and may disrupt communications on the L-Net run |