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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 1 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Codan | BC 262 | FDA UDI | Class II | Active |
| Walrus | B 429-W | FDA UDI | Class II | Active |
| Medical Systems | 901100 | FDA UDI | Class II | Active |
| Codan | LS 417 | FDA UDI | Class II | Active |
| Codan | A327 | FDA UDI | Class II | Active |
| Codan | BC1118 | FDA UDI | Class II | Active |
| Codan | EF 132-OS | FDA UDI | Class II | Active |
| Codan | BC 517 | FDA UDI | Class II | Active |
| Codan | B 411 | FDA UDI | Class II | Active |
| Codan | BC 2153 | FDA UDI | Class II | Active |
| Codan | B 418N | FDA UDI | Class II | Active |
| Codan | BC 513 | FDA UDI | Class II | Active |
| Codan | BC 2019 | FDA UDI | Class II | Active |
| Codan | BC2186 | FDA UDI | Class II | Active |
| Codan | DEN-D | FDA UDI | Class II | Active |
| Walrus | W22402 | FDA UDI | Class II | Active |
| Codan | C 301 | FDA UDI | Class II | Active |
| Codan | BC 2093 | FDA UDI | Class II | Active |
| Codan | BC 608 | FDA UDI | Class II | Active |
| Codan | 92062-1100 | FDA UDI | Class II | Active |
| Codan | BC 2046 | FDA UDI | Class II | Active |
| Walrus | W20171 | FDA UDI | Class II | Active |
| Label Product -codan | BC 263 | FDA UDI | Class II | Active |
| Codan | BC2161 | FDA UDI | Class II | Active |
| Walrus | BC 298-W | FDA UDI | Class II | Active |
| Codan | BC 2081 | FDA UDI | Class II | Active |
| Codan | BC 294 | FDA UDI | Class II | Active |
| Codan | C 407-W | FDA UDI | Class II | Active |
| Codan | BC 560 | FDA UDI | Class II | Active |
| Codan | BC 5954 | FDA UDI | Class II | Active |
| Codan | ETT-A-1550.13 | FDA UDI | Class II | Active |
| Walrus | BASN-NS/150 | FDA UDI | Class II | Active |
| Codan | BC 277 | FDA UDI | Class II | Active |
| Walrus | A 807-W | FDA UDI | Class II | Active |
| Walrus | BC 2060-W | FDA UDI | Class II | Active |
| Walrus | W20322 | FDA UDI | Class II | Active |
| Codan | LS 415N | FDA UDI | Class II | Active |
| Codan | MSRV-1428 | FDA UDI | Class II | Active |
| Codan | BC 518 | FDA UDI | Class II | Active |
| Codan | A 315 | FDA UDI | Class II | Active |
| Walrus | W21441 | FDA UDI | Class II | Active |
| Codan | W 22374 | FDA UDI | Class II | Active |
| Codan | C 354N | FDA UDI | Class II | Active |
| Safti-Ject | BC 6004 | FDA UDI | Class II | Active |
| Codan | W21745-W | FDA UDI | Class II | Active |
| Codan | A611 | FDA UDI | Class II | Active |
| Codan | A 806-W | FDA UDI | Class II | Active |
| Codan | BC 574 | FDA UDI | Class II | Active |
| Codan | BC 2084 | FDA UDI | Class II | Active |
| Kabi Access Infusion Sets | FK70110K | 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. |