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Sign in to claim this brandNORTH AMERICAN RESCUE, LLC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 35 TEDWALL COURT, Greer, SC, 29650
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 6 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-1081 | FDA UDI | N/A | Active |
| Nar | 85-4919 | FDA UDI | Class I | Active |
| Nar | 85-4433 | FDA UDI | N | Active |
| Nar | 85-4547 | FDA UDI | N | Active |
| NAR Kit | 85-3218 | FDA UDI | N/A | Active |
| NAR Kit | 85-3077 | FDA UDI | N/A | Active |
| Nar | 85-4176 | FDA UDI | N/A | Active |
| Nar | 85-2441 | FDA UDI | N/A | Active |
| Nar | 85-4502 | FDA UDI | Class II | Active |
| Nar | 80-0939 | FDA UDI | N/A | Active |
| NAR Kit | 85-2356 | FDA UDI | N/A | Active |
| NAR Kit | 85-3408 | FDA UDI | N/A | Active |
| Nar | 85-4420 | FDA UDI | N | Active |
| Nar | 85-4787 | FDA UDI | N | Active |
| NAR Kit | 85-3647 | FDA UDI | N/A | Active |
| Nar | 80-0935 | FDA UDI | N/A | Active |
| NAR Kit | 85-1725 | FDA UDI | N/A | Active |
| Nar | 85-1647 | FDA UDI | N/A | Active |
| Nar | 80-1665 | FDA UDI | Class I | Active |
| Nar | 80-1439 | FDA UDI | N | Active |
| NAR Kit | 85-1891 | FDA UDI | N/A | Active |
| Nar | 85-4237 | FDA UDI | N/A | Active |
| Nar | 85-3877 | FDA UDI | N/A | Active |
| Nar | 85-3124 | FDA UDI | N/A | Active |
| NAR Kit | 80-0245 | FDA UDI | N/A | Active |
| NAR Kit | 85-2663 | FDA UDI | N/A | Active |
| NAR Kit | 80-0462 | FDA UDI | N/A | Active |
| Nar | 85-4909 | FDA UDI | Class I | Active |
| Nar | 80-1054 | FDA UDI | N/A | Active |
| Nar | 85-4596 | FDA UDI | Class I | Active |
| Nar | 85-3777 | FDA UDI | N/A | Active |
| NAR Kit | 85-2304 | FDA UDI | N/A | Active |
| NAR Kit | 85-1048 | FDA UDI | N/A | Active |
| Nar | 85-1939 | FDA UDI | N/A | Active |
| Nar | 80-1082 | FDA UDI | N/A | Active |
| Nar | 85-4867 | FDA UDI | Class I | Active |
| Nar | 85-3171 | FDA UDI | N/A | Active |
| Nar | 85-3983 | FDA UDI | N/A | Active |
| Nar | 85-4528 | FDA UDI | Class I | Active |
| NAR Kit | 80-0093 | FDA UDI | N/A | Active |
| Nar | 84-0135 | FDA UDI | N/A | Active |
| NAR Kit | 85-2264 | FDA UDI | N/A | Unknown |
| Nar | 30-0054 | FDA UDI | Class I | Active |
| Nar | 85-2883 | FDA UDI | N/A | Active |
| NAR Kit | 70-0196 | FDA UDI | N/A | Active |
| Nar | 85-0556 | FDA UDI | N/A | Active |
| Nar | 85-4847 | FDA UDI | Class I | Active |
| Nar | 85-4012 | FDA UDI | N/A | Active |
| Nar | 85-3217 | FDA UDI | N/A | Active |
| NAR Kit | 85-2601 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (4)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 27, 2026 | Z-1947-2026 | — | open, classified | Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the meter displays an E-5 error code for a very high blood glucose event (> 600 mg/dL) or when there is a test strip error, which can lead to operator confusion when evaluating patients and a delay in appropriate treatment. This is a downstream recall of Trividia Health Class I, Recall Event ID 98317. |
| Jul 1, 2025 | Z-2637-2025 | — | open, classified | Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use. |
| Aug 27, 2021 | Z-2520-2021 | — | terminated | The device includes the incorrect Instructions for Use. |
| Aug 21, 2020 | Z-3018-2020 | — | terminated | Lack of sterility assurance of the 30-0171 |