International Medical Devices Database

Manufacturer Parent Company (2017)
Coloplast A/S
Source
AEMPSVFOI
1 Event
- Recall Or Safety Alert for Vortek® single-curvature ureteral stent, ref: ACA106, ACA107, ACA108, ACA206, ACA207 and ACA208.

One device in the database

Vortek® single-curvature ureteral stent, ref: ACA106, ACA107, ACA108, ACA206, ACA207 and ACA208.

Model / Serial

20 manufacturers with a similar name

Learn more about the data here

Coloplast A/S

Manufacturer Parent Company (2017)
Coloplast A/S
Source
NIDFSINVIMA

Coloplast A/S

Manufacturer Parent Company (2017)
Coloplast A/S
Source
AFOSHCBASG

Coloplast A/S

Manufacturer Parent Company (2017)
Coloplast A/S
Source
NZMMDSA

COLOPLAST A/S

Manufacturer Parent Company (2017)
Coloplast A/S
Source
MSHM

Coloplast A/S.

Manufacturer Parent Company (2017)
Coloplast A/S
Source
AEMPSVFOI

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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