International Medical Devices Database

Manufacturer Parent Company (2017)
Coloplast A/S
Source
RLMPH
2 Events
- Recall of Biatain Ag Cavity Filler
- Recall of Restorelle DirectFix Anterior, Restorelle DirectFix Posterior, and Altis Single Incision Sling

2 devices in the database

Restorelle DirectFix Anterior, Restorelle DirectFix Posterior, and Altis S...

Model / Serial

One manufacturer with a similar name

Learn more about the data here

Coloplast Pty Ltd

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

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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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Coloplast Pty Ltd

2 devices in the database

Biatain Ag Cavity Filler

Restorelle DirectFix Anterior, Restorelle DirectFix Posterior, and Altis S...

One manufacturer with a similar name

Coloplast Pty Ltd