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Sign in to claim this brandCODAN US Corporation
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2001 Sanyo Avenue Suite 130, San Diego, CA, 92154
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 3020417125
- DUNS Number
- —
Catalogue (728)
Page 7 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Codan | BC 729 | FDA UDI | Class II | Active |
| Kabi Access Infusion Sets | FK20219KE | FDA UDI | Class II | Active |
| Codan | B 8015-W | FDA UDI | Class II | Active |
| Codan | A612 | FDA UDI | Class II | Active |
| Codan | BC 2059-W | FDA UDI | Class II | Active |
| Codan | B 315 | FDA UDI | Class II | Active |
| Codan | BC 594 | FDA UDI | Class II | Active |
| Codan | A 602 | FDA UDI | Class II | Active |
| Codan | BMJ-35-NSP | FDA UDI | Class II | Active |
| Codan | BC 688 | FDA UDI | Class II | Active |
| Codan | BC 278-EM | FDA UDI | Class II | Active |
| Codan | BC1114 | FDA UDI | Class II | Active |
| Codan Cyto | CYTO-21V | FDA UDI | Class II | Active |
| Safti-Ject | BC 1024 | FDA UDI | Class II | Active |
| Codan | 1018514 | FDA UDI | Class II | Active |
| Codan | BC 2072 | FDA UDI | Class II | Active |
| Codan | BC 2037-W | FDA UDI | Class II | Active |
| Walrus by CODAN | A 817-W | FDA UDI | Class II | Active |
| Codan | BC 258 | FDA UDI | Class II | Active |
| Codan | W20139 | FDA UDI | Class II | Active |
| Codan | 25.7192 | FDA UDI | Class II | Active |
| Codan | A463 | FDA UDI | Class II | Active |
| Codan | C 443 | FDA UDI | Class II | Active |
| Walrus | A 814-W | FDA UDI | Class II | Active |
| Codan | BC 581 | FDA UDI | Class II | Active |
| Codan | BC 2118 | FDA UDI | Class II | Active |
| Walrus | B 435-W | FDA UDI | Class II | Active |
| Codan | BC 239N | FDA UDI | Class II | Active |
| Codan | B 863 | FDA UDI | Class II | Active |
| Codan | EF 114 | FDA UDI | Class II | Active |
| Codan | BC 2086 | FDA UDI | Class II | Active |
| Codan | W20214 | FDA UDI | Class II | Active |
| Codan | BC 108 | FDA UDI | Class II | Active |
| Codan | C 32C | FDA UDI | Class II | Active |
| Codan | A485 | FDA UDI | Class II | Active |
| Codan | BC 2112 | FDA UDI | Class II | Active |
| Codan | BC 590 | FDA UDI | Class II | Active |
| Codan | BC 2135 | FDA UDI | Class II | Active |
| Codan | BC 201 | FDA UDI | Class II | Active |
| Ima | BC 274 | FDA UDI | Class II | Active |
| Codan | C 368 | FDA UDI | Class II | Active |
| Codan | A 492 | FDA UDI | Class II | Active |
| Codan | BC 2018-W | FDA UDI | Class II | Active |
| Codan | B 310 | FDA UDI | Class II | Active |
| Codan | BC 2083 | FDA UDI | Class II | Active |
| Codan | B 492 | FDA UDI | Class II | Active |
| Fresenius Kabi | FK20256KE | FDA UDI | Class II | Active |
| Codan | BC 301 | FDA UDI | Class II | Active |
| Codan | W20267 | FDA UDI | Class II | Active |
| Codan | 1017080 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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Authorities
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FDA Recalls (2)
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 |
|---|---|---|---|---|
| Sep 12, 2019 | Z-2433-2020 | — | terminated | Individual packages of connectors may have incomplete or bad seals which would compromise sterility. |
| Aug 17, 2011 | Z-2040-2014 | — | terminated | CODAN US Corporation is recalling the ColorSafe IV (intravenous) product lines because they were manufactured and marketed prior to FDA approval. |