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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2246340
- DUNS Number
- —
Catalogue (55)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ScatPad | SMA 123 | FDA UDI | Class I | Active |
| ScatPad | SEPA 442 | FDA UDI | Class I | Active |
| Cardio Clear | LTA202 | FDA UDI | Class II | Active |
| Cardio Clear | LOCH504 | FDA UDI | Class II | Active |
| Cardio Clear | PA302 | FDA UDI | Class II | Active |
| ScatPad | SAFA 301 | FDA UDI | Class I | Active |
| ScatPad | SEPA 412 | FDA UDI | Class I | Active |
| Cardio Clear | LOCO501 | FDA UDI | Class II | Active |
| Cardio Clear | P103 | FDA UDI | Class II | Active |
| Cardio Clear | O101 | FDA UDI | Class II | Active |
| Cardio Clear | O101-S | FDA UDI | Class II | Active |
| Cardio Clear | O401 | FDA UDI | Class II | Active |
| Cardio Clear | A102 | FDA UDI | Class II | Active |
| Cardio Clear | H104 | FDA UDI | Class II | Active |
| Cardio Clear | PH304 | FDA UDI | Class II | Active |
| Cardio Clear | LZ100-S | FDA UDI | Class II | Active |
| Cardio Clear | TA202 | FDA UDI | Class II | Active |
| Cardio Clear | LOCZ500 | FDA UDI | Class II | Active |
| ScatPad | SEPA 453-X | FDA UDI | Class I | Active |
| Cardio Clear | TO201 | FDA UDI | Class II | Active |
| Cardio Clear | LTH204 | FDA UDI | Class II | Active |
| Cardio Clear | TH204 | FDA UDI | Class II | Active |
| ScatPad | SEPA 403-CTRSCP | FDA UDI | Class I | Active |
| Cardio Clear | PZ300 | FDA UDI | Class II | Active |
| Cardio Clear | Z400 | FDA UDI | Class II | Active |
| ScatPad | SAFA 302 | FDA UDI | Class I | Active |
| Cardio Clear | LZ100 | FDA UDI | Class II | Active |
| ScatPad | SDFA 701 | FDA UDI | Class I | Active |
| Cardio Clear | A402 | FDA UDI | Class II | Active |
| Cardio Clear | P403 | FDA UDI | Class II | Active |
| ScatPad | SEPA 463-X-AF | FDA UDI | Class I | Active |
| ScatPad | SEPA 402-A | FDA UDI | Class I | Active |
| Cardio Clear | PO301 | FDA UDI | Class II | Active |
| ScatPad | SDFA 702 | FDA UDI | Class I | Active |
| ScatPad | STSN 802 | FDA UDI | Class I | Active |
| Cardio Clear | LTP203 | FDA UDI | Class II | Active |
| Cardio Clear | H404 | FDA UDI | Class II | Active |
| Cardio Clear | LTZ200 | FDA UDI | Class II | Active |
| ScatPad | SEPA 402-DT | FDA UDI | Class I | Active |
| ScatPad | SPA 501 | FDA UDI | Class I | Active |
| Cardio Clear | LOCA502 | FDA UDI | Class II | Active |
| Cardio Clear | TZ200 | FDA UDI | Class II | Active |
| Cardio Clear | PP303 | FDA UDI | Class II | Active |
| Cardio EP LED Headlight | 1 | FDA UDI | Class I | Active |
| Cardio Clear | Z100 | FDA UDI | Class II | Active |
| ScatPad | SPA 502 | FDA UDI | Class I | Active |
| Cardio Clear | TP203 | FDA UDI | Class II | Active |
| Cardio Clear | LTO201 | FDA UDI | Class II | Active |
| ScatPad | SJAA 601-X | FDA UDI | Class I | Active |
| ScatPad | SAPA 401 | FDA UDI | Class I | Active |
Related Companies
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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. |