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Sign in to claim this brandNucryo Vascular
US
Last updated May 27, 2026
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 045796615
Catalogue (35)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| PolarCath | T254015001 | FDA UDI | Class II | Active |
| PolarCath | T6010013501 | FDA UDI | Class II | Active |
| PolarCath | P54012001 | FDA UDI | Class II | Active |
| PolarCath | T3010015001 | FDA UDI | Class II | Active |
| PolarCath | T5010013501 | FDA UDI | Class II | Active |
| PolarCath | T6015013501 | FDA UDI | Class II | Active |
| PolarCath | T404015001 | FDA UDI | Class II | Active |
| PolarCath | P415012001 | FDA UDI | Class II | Active |
| PolarCath | T354015001 | FDA UDI | Class II | Active |
| PolarCath | T204015001 | FDA UDI | Class II | Active |
| PolarCath | P84012001 | FDA UDI | Class II | Active |
| PolarCath | T4010015001 | FDA UDI | Class II | Active |
| PolarCath | T3510015001 | FDA UDI | Class II | Active |
| PolarCath | T504013501 | FDA UDI | Class II | Active |
| PolarCath | T2515015001 | FDA UDI | Class II | Active |
| PolarCath | T4015015001 | FDA UDI | Class II | Active |
| PolarCath | NC3000001 | FDA UDI | Class II | Active |
| PolarCath | P610012001 | FDA UDI | Class II | Active |
| PolarCath | P615012001 | FDA UDI | Class II | Active |
| PolarCath | T5015013501 | FDA UDI | Class II | Active |
| PolarCath | T2010015001 | FDA UDI | Class II | Active |
| PolarCath | P44012001 | FDA UDI | Class II | Active |
| PolarCath | P510012001 | FDA UDI | Class II | Active |
| PolarCath | P64012001 | FDA UDI | Class II | Active |
| PolarCath | T2510015001 | FDA UDI | Class II | Active |
| PolarCath | T304015001 | FDA UDI | Class II | Active |
| PolarCath | T3515015001 | FDA UDI | Class II | Active |
| PolarCath | T2015015001 | FDA UDI | Class II | Active |
| PolarCath | P515012001 | FDA UDI | Class II | Active |
| PolarCath | P74012001 | FDA UDI | Class II | Active |
| PolarCath | P410012001 | FDA UDI | Class II | Active |
| CryoPlasty | PCIU500000 | FDA UDI | Class II | Active |
| PolarCath | T3015015001 | FDA UDI | Class II | Active |
| PolarCath | PCE1000000 | FDA UDI | Class II | Active |
| PolarCath | T604013501 | FDA UDI | Class II | 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 |
|---|---|---|---|---|
| Oct 11, 2019 | Z-0507-2020 | — | terminated | Peripheral Dilation Catheters that were E-Beam Sterilized were inadvertently mislabeled with EO sterilized labels. |