William Cook Europe ApS
US Last updated 24 May 2026
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- Devices
- 442
- Registries
- GUDIDEUDAMEDFDA
- FDA recalls
- 0
Catalogue
Cook G47467 Ref G47467
Zenith Alpha G35328 Ref G35328
Zenith Alpha G35514 Ref G35514
Cook G47445 Ref G47445
Cook G53517 Ref G53517
Zenith TX2 Pro-Form G53484 Ref G53484
Zenith Alpha G38041 Ref G38041
Zenith Alpha G60055 Ref G60055
Cook Celect G52915 Ref G52915
Formula G56971 Ref G56971
Zenith TX2 Pro-Form G53474 Ref G53474
Gunther Tulip G52916 Ref G52916
MReye Flipper G48354 Ref G48354
Zenith Alpha G35391 Ref G35391
Cook G47471 Ref G47471
Zenith Alpha G38055 Ref G38055
Formula G56963 Ref G56963
Formula G56966 Ref G56966
Lunderquist G49235 Ref G49235
Zenith Alpha G35507 Ref G35507
Cook G47472 Ref G47472
Zenith Alpha G60142 Ref G60142
Cook G47465 Ref G47465
Cook G23646 Ref G23646
Flipper G12913 Ref G12913
Cook G47439 Ref G47439
Zenith Alpha G60157 Ref G60157
Zenith Alpha G60180 Ref G60180
Cook Celect G34309 Ref G34309
Gunther Tulip G52917 Ref G52917
Zenith Alpha G60154 Ref G60154
Cook G47468 Ref G47468
Zenith Alpha G38236 Ref G38236
Zenith Alpha G60171 Ref G60171
Zenith Alpha G60040 Ref G60040
Lunderquist G49229 Ref G49229
Zenith Alpha G35510 Ref G35510
Zenith TX2 Pro-Form G53482 Ref G53482
Zenith Alpha G35365 Ref G35365
Formula G56968 Ref G56968
Formula G56959 Ref G56959
MReye Flipper G48358 Ref G48358
Zenith Alpha G35509 Ref G35509
Zenith Alpha G38216 Ref G38216
Formula G18525 Ref G18525
Lunderquist G49227 Ref G49227
Zenith Alpha G35402 Ref G35402
Zenith TX2 Pro-Form G53486 Ref G53486
Cook G47444 Ref G47444
Cook G47461 Ref G47461
Showing 1-50 of 442
FDA establishments
- William Cook Europe Aps BJAEVERSKOV Sjaelland · DK FEI 3002808486
What William Cook Europe ApS makes
William Cook Europe ApS manufactures synthetic vascular grafts for vascular reconstruction, as well as single-use guidewires designed for cardiac and peripheral vascular procedures. Their portfolio includes non-neurovascular embolization coils and vena cava filters, both temporary and permanent, alongside bare-metal aortic stents for vascular interventions. The company also produces endotracheal tube introducers for single-use medical applications and specialized tools like embolization implant inserters.
The company’s devices are classified under FDA’s Class II and Class III categories, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, where regulatory compliance follows FDA requirements for medical devices. The company is based in the US, adhering to applicable domestic and international regulatory standards for their respective device classes.
Information
- Country
- US
- Website
- cookmedical.com
- [email protected]
- Phone
- +1(812)330-5494
- DUNS number
- 305302119