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United States·US-MF-000044140
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 333, Fuller Ave NE, Grand Rapids, United States
- Website
- www.marmed.com
- —
- —
- [email protected]
- Phone
- +1 616 454 3000
- PRRC Contact
- Joel Marogil
- EUDAMED SRN
- US-MF-000044140
- FDA FEI Number
- 1832653
- DUNS Number
- —
Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tourni-Cot - Large | TCL | FDA UDI | Class I | Active |
| Rhino-Pak 45mm | RP-45 | FDA UDI | Class I | Active |
| Derma-Stent | DMT | FDA UDI | Class I | Active |
| Rhino-Pak 55mm | RP-55 | FDA UDI | Class I | Active |
| Balloon Extractor | BEX | FDA UDI | Class I | Active |
| Tourni-Cot - Universal | TCU | FDA UDI | Class I | Active |
| Tourni-Cot - Medium | TCM | FDA UDI | Class I | Active |
| Tourni-Cot - Extra Large | TXL | EUDAMEDFDA UDI | Class I | Active |
| ZeroWet | Klenzalac | FDA UDI | Class I | Active |
| ZeroWet | SuperShield | FDA UDI | Class I | Active |
| Tourni-Cot - Small | TCS | FDA UDI | Class I | Active |
| Rhino-Pak 75mm | RP-75 | FDA UDI | Class I | Active |
| Mar-Med Liver Strap | K924223 | FDA 510(k) | 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 |
|---|---|---|---|---|
| Dec 28, 2020 | Z-0945-2021 | — | terminated | A failure can occur if the user attempts to remove the device by partially snipping the edge and pulling on it. The device may tear into two pieces with a portion remaining in place, which can continue to constrict the vessels. This type of failure can result in digit ischemia. |