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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 49 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-2069 | FDA UDI | N/A | Active |
| Nar | 77-0087 | FDA UDI | N | Active |
| Nar | 85-2783 | FDA UDI | N/A | Active |
| Nar | 85-4212 | FDA UDI | N/A | Active |
| Nar | 85-0665 | FDA UDI | N/A | Active |
| Nar | 85-4380 | FDA UDI | Class I | Active |
| Nar | 80-1675 | FDA UDI | Class I | Active |
| NAR Kit | 85-1840 | FDA UDI | N/A | Active |
| Nar | 85-1259 | FDA UDI | N/A | Active |
| Nar | 88-0005 | FDA UDI | Class I | Active |
| NAR Kit | 80-0047 | FDA UDI | N/A | Active |
| Nar | 80-0418-TLS | FDA UDI | Class I | Active |
| NAR Kit | 80-0048 | FDA UDI | N/A | Active |
| Nar | 85-3301 | FDA UDI | N/A | Active |
| Nar | 85-3789 | FDA UDI | N/A | Active |
| Nar | 80-0468 | FDA UDI | N/A | Active |
| Nar | 85-1677 | FDA UDI | N/A | Active |
| Nar | 85-3497 | FDA UDI | N/A | Active |
| Nar | 85-4721 | FDA UDI | Class I | Active |
| Nar | 85-4106 | FDA UDI | N/A | Active |
| Nar | 85-3912 | FDA UDI | N/A | Active |
| NAR Kit | 85-2610 | FDA UDI | N/A | Active |
| Nar | 85-3494 | FDA UDI | N/A | Active |
| Nar | 85-1454 | FDA UDI | N/A | Active |
| Nar | 84-0118 | FDA UDI | N/A | Active |
| NAR Kit | 10-0003 | FDA UDI | Class I | Active |
| Nar | 80-1177 | FDA UDI | N/A | Active |
| Nar | 85-3100 | FDA UDI | N/A | Active |
| NAR Kit | 85-3661 | FDA UDI | N/A | Active |
| NAR Kit | 80-0466 | FDA UDI | N/A | Active |
| NAR Kit | 85-1639 | FDA UDI | N/A | Active |
| Nar | 85-2605 | FDA UDI | N/A | Active |
| Nar | 85-2627 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-0776 | FDA UDI | N/A | Active |
| Nar | 87-0002 | FDA UDI | Class I | Active |
| Nar | 80-1828 | FDA UDI | N | Active |
| NAR Kit | 85-2233 | FDA UDI | N/A | Active |
| Nar | 80-1502 | FDA UDI | N/A | Active |
| Nar | 85-3421 | FDA UDI | N/A | Active |
| Nar | 85-3295 | FDA UDI | N/A | Active |
| Nar | 88-0035 | FDA UDI | Class I | Active |
| Nar | 85-4113 | FDA UDI | N/A | Active |
| Nar | 85-2439 | FDA UDI | N/A | Active |
| Nar | 85-3132 | FDA UDI | Class I | Active |
| Nar | 85-4736 | FDA UDI | Class I | Active |
| Nar | 80-0936 | FDA UDI | N/A | Active |
| Nar | 85-4527 | FDA UDI | Class I | Active |
| NAR Kit | 85-3021 | FDA UDI | N/A | Active |
| NAR Kit | 85-3592 | FDA UDI | N/A | Active |
| NAR Kit | 85-0662 | 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 |