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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
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020417125
- DUNS Number
- —
Catalogue (728)
Page 2 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Codan | BC 2091 | FDA UDI | Class II | Active |
| Codan | BC 713 | FDA UDI | Class II | Active |
| Msd | MS 421 | FDA UDI | Class II | Active |
| Codan | W21902 | FDA UDI | Class II | Active |
| Codan | B 4164 | FDA UDI | Class II | Active |
| Codan | W20366 | FDA UDI | Class II | Active |
| Codan | B 424 | FDA UDI | Class II | Active |
| Codan | BC 589 | FDA UDI | Class II | Active |
| Kabi Access Infusion Sets | FK70100K | FDA UDI | Class II | Active |
| Codan | BC 523N | FDA UDI | Class II | Active |
| Codan | 1018517 | FDA UDI | Class II | Active |
| Codan | C 350 | FDA UDI | Class II | Active |
| Codan | LS 689 | FDA UDI | Class II | Active |
| Codan | B 805 | FDA UDI | Class II | Active |
| Codan | BC2166 | FDA UDI | Class II | Active |
| Codan | C 424 | FDA UDI | Class II | Active |
| Codan | EF 122-OS | FDA UDI | Class II | Active |
| Walrus | BASNUM-60/150 | FDA UDI | Class II | Active |
| Codan | BC 583 | FDA UDI | Class II | Active |
| Codan | C 2002-W | FDA UDI | Class II | Active |
| Codan | BC 200 | FDA UDI | Class II | Active |
| Codan | BMJ-35 | FDA UDI | Class II | Active |
| Codan | AB 302 | FDA UDI | Class II | Active |
| Codan | BC 265 | FDA UDI | Class II | Active |
| Chr. Hansen | CH 610 422 | FDA UDI | Class II | Active |
| Codan | BC 2050-TF | FDA UDI | Class II | Active |
| Light-Safe | LS 230 | FDA UDI | Class II | Active |
| Codan | W21114 | FDA UDI | Class II | Active |
| Codan | C 805 | FDA UDI | Class II | Active |
| Fresenius Kabi | FK40100KT | FDA UDI | Class II | Active |
| Codan | BC 102 Special | FDA UDI | Class II | Active |
| Fresenius Kabi | FK20203KE | FDA UDI | Class II | Active |
| Walrus | B 8007-W | FDA UDI | Class II | Active |
| Codan | BC 2098 | FDA UDI | Class II | Active |
| Codan | BC 546R | FDA UDI | Class II | Active |
| Walrus | A 900-W | FDA UDI | Class II | Active |
| Walrus | A 2010-W | FDA UDI | Class II | Active |
| Codan | B2022-W | FDA UDI | Class II | Active |
| Codan | B 5301 | FDA UDI | Class II | Active |
| Codan | C 850 | FDA UDI | Class II | Active |
| Fresenius Kabi | FK20251KE | FDA UDI | Class II | Active |
| Codan | BC 264 | FDA UDI | Class II | Active |
| Codan | DEN-SB | FDA UDI | Class II | Active |
| HealthMark | TS 350 | FDA UDI | Class II | Active |
| Codan | C 411 | FDA UDI | Class II | Active |
| Codan | BC 2065 | FDA UDI | Class II | Active |
| Codan | BC 2012-W | FDA UDI | Class II | Active |
| Codan | BC1112 | FDA UDI | Class II | Active |
| Codan | B 496-W | FDA UDI | Class II | Active |
| Codan | BC 561 | FDA UDI | Class II | Active |
Related Companies
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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. |