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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 26 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 80-0495 | FDA UDI | N/A | Active |
| Nar | 85-3078 | FDA UDI | N/A | Active |
| Nar | 85-1908 | FDA UDI | N/A | Active |
| NAR Kit | 85-3407 | FDA UDI | N/A | Active |
| Nar | 85-1819 | FDA UDI | Class I | Active |
| NAR Kit | 85-3522 | FDA UDI | N/A | Active |
| NAR Kit | 85-2808 | FDA UDI | N/A | Active |
| Nar | 85-4559 | FDA UDI | N | Active |
| Nar | 85-2281 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-0034 | FDA UDI | Class I | Active |
| Nar | 85-4801 | FDA UDI | Class I | Active |
| Nar | 85-4387 | FDA UDI | Class I | Active |
| Nar | 80-1456 | FDA UDI | Class I | Active |
| Nar | 85-4079 | FDA UDI | N/A | Active |
| NAR Kit | 80-1146 | FDA UDI | N/A | Active |
| Nar | 85-4516 | FDA UDI | Class I | Active |
| Nar | 85-2839 | FDA UDI | N/A | Active |
| NAR Kit | 80-0984 | FDA UDI | N/A | Active |
| Nar | 80-1171 | FDA UDI | N/A | Active |
| Nar | 80-1481 | FDA UDI | N/A | Active |
| NAR Kit | 85-3210 | FDA UDI | N/A | Active |
| Nar | 85-2915 | FDA UDI | N/A | Active |
| Nar | 85-4421 | FDA UDI | Class I | Active |
| NAR Kit | 85-0191 | FDA UDI | N/A | Active |
| Nar | 85-1385 | FDA UDI | N/A | Active |
| Nar | 30-0179 | FDA UDI | Class I | Active |
| Nar | 85-4932 | FDA UDI | Class I | Active |
| NAR Kit | 85-1745 | FDA UDI | N/A | Active |
| Nar | 85-3655 | FDA UDI | N/A | Active |
| Nar | 85-3779 | FDA UDI | N/A | Active |
| Nar | 85-4578 | FDA UDI | Class I | Active |
| Nar | 85-2510 | FDA UDI | N/A | Active |
| Nar | 85-3147 | FDA UDI | N/A | Active |
| NAR Kit | 80-0004 | FDA UDI | N/A | Active |
| NAR Kit | 85-3470 | FDA UDI | N/A | Active |
| Nar | 80-1753 | FDA UDI | Class I | Active |
| Nar | 80-0952 | FDA UDI | N/A | Active |
| Nar | 80-0996 | FDA UDI | N/A | Active |
| Nar | 85-2275 | FDA UDI | N/A | Active |
| NAR Kit | 80-0159 | FDA UDI | N/A | Active |
| Nar | 80-0879 | FDA UDI | N/A | Active |
| NAR Kit | 85-1355 | FDA UDI | N/A | Active |
| Nar | 80-1739 | FDA UDI | Class I | Active |
| Nar | 80-1477 | FDA UDI | N/A | Active |
| NAR Kit | 85-2931 | FDA UDI | N/A | Active |
| NAR Kit | 85-1412 | FDA UDI | N/A | Active |
| NAR Kit | 85-3673 | FDA UDI | N/A | Active |
| Nar | 85-3511 | FDA UDI | N/A | Active |
| Nar | 85-3910 | FDA UDI | N/A | Active |
| Nar | 85-3710 | FDA UDI | N/A | Active |
Related Companies
Authorised Representatives
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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 |