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Sign in to claim this brandMARINA MEDICAL INSTRUMENTS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 8190 West State Road 84, Davie, FL, 33324
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000124817
- DUNS Number
- —
Catalogue (3681)
Page 67 of 74| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Marina Medical | 050-350SC | FDA UDI | Class I | Active |
| Marina Medical | 252-009 | FDA UDI | Class I | Active |
| Marina Medical | 110-393 | FDA UDI | Class I | Active |
| Marina Medical | 070-355XL | FDA UDI | Class I | Active |
| Marina Medical | 110-058 | FDA UDI | Class I | Active |
| Marina Medical | 200-166 | FDA UDI | Class I | Active |
| Marina Medical | 161-541 | FDA UDI | Class I | Active |
| Marina Medical | 280-503 | FDA UDI | Class I | Active |
| Marina Medical | 420-878 | FDA UDI | Class I | Active |
| Marina Medical | BM2.25S | FDA UDI | Class II | Active |
| Marina Medical | 110-392 | FDA UDI | Class I | Active |
| Marina Medical | 170-130 | FDA UDI | Class I | Active |
| Marina Medical | 110-867 | FDA UDI | Class I | Active |
| Marina Medical | 310-891 | FDA UDI | Class I | Active |
| Marina Medical | 800-100 | FDA UDI | Class I | Active |
| Marina Medical | 410-126 | FDA UDI | Class I | Active |
| Marina Medical | 020-073 | FDA UDI | Class I | Active |
| Marina Medical | 080-100 | FDA UDI | Class I | Active |
| Marina Medical | 330-325XL | FDA UDI | Class I | Active |
| Marina Medical | 310-460 | FDA UDI | Class I | Active |
| Marina Medical | 300-024 | FDA UDI | Class I | Active |
| Marina Medical | 070-314 | FDA UDI | Class I | Active |
| Marina Medical | 120-701L | FDA UDI | Class I | Active |
| Marina Medical | 410-230 | FDA UDI | Class I | Active |
| Marina Medical | 280-200R | FDA UDI | Class I | Active |
| Marina Medical | 600-267 | FDA UDI | Class I | Active |
| Marina Medical | 300-124 | FDA UDI | Class I | Active |
| Marina Medical | 200-136 | FDA UDI | Class I | Active |
| Marina Medical | 060-364 | FDA UDI | Class I | Active |
| Marina Medical | 070-556 | FDA UDI | Class I | Active |
| Marina Medical | 201-042 | FDA UDI | Class I | Active |
| Marina Medical | 800-815 | FDA UDI | Class II | Active |
| Marina Medical | 200-222 | FDA UDI | Class I | Active |
| Marina Medical | 380-590 | FDA UDI | Class I | Active |
| Marina Medical | 180-025NS | FDA UDI | Class II | Active |
| Marina Medical | 270-304 | FDA UDI | Class I | Active |
| Marina Medical | 190-392 | FDA UDI | Class I | Active |
| Marina Medical | 110-845 | FDA UDI | Class I | Active |
| Marina Medical | 440-312 | FDA UDI | Class I | Active |
| Marina Medical | 042-042 | FDA UDI | Class I | Active |
| Marina Medical | 201-062 | FDA UDI | Class I | Active |
| Marina Medical | 060-524A-NC | FDA UDI | Class I | Active |
| Marina Medical | 172-618 | FDA UDI | Class I | Active |
| Marina Medical | MM-TIPA8 | FDA UDI | Class I | Active |
| Marina Medical | BR3.50 | FDA UDI | Class II | Active |
| Marina Medical | 336-802 | FDA UDI | Class I | Active |
| Marina Medical | 250-303LS | FDA UDI | Class I | Active |
| Marina Medical | 420-456LH | FDA UDI | Class I | Active |
| Marina Medical | 190-704XL | FDA UDI | Class I | Active |
| Marina Medical | 110-100 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (3)
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 9, 2009 | Z-1208-2010 | — | terminated | Marina Medical, Sunrise, FL initiated recall of 46 products of 350 series devices and 47 products of 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation. |
| Apr 9, 2009 | Z-1206-2010 | — | terminated | Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation. |
| Apr 9, 2009 | Z-1207-2010 | — | terminated | Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation. |