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Sign in to claim this brandCARDIO MEDICAL PRODUCTS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 385 Franklin Ave Ste L, ROCKAWAY, NJ, 07866
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2246340
- DUNS Number
- —
Catalogue (55)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cardio Clear | LOCP503 | FDA UDI | Class II | Active |
| ScatPad | SMA 102 | FDA UDI | Class I | Active |
| Cardiomed | K103651 | FDA 510(k) | Class II | Active |
| Cardio Med | K103334 | FDA 510(k) | Class II | Active |
| Cardio Med Model A102, H104, O101, P103, And Z100 | K103159 | FDA 510(k) | Class II | Active |
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 26, 2013 | Z-1669-2013 | — | terminated | Covidien received customer reports of Arcing/Sparking on the defibrillation electrode leadwire which may affect Cardio Medical Products Inc. defibrillator electrodes Model Number O101. |