Devices

Restorelle DirectFix Anterior, Restorelle DirectFix Posterior, and Altis Single Incision Sling

Model / Serial
Restorelle DirectFix Anterior, Restorelle DirectFix Posterior, and Altis Single Incision SlingRestorelle DirectFix AnteriorModel/Catalogue Number: 501450SKU Number: 5014501022ARTG 190172Restorelle DirectFix PosteriorModel/Catalogue Number: 501460SKU Number: 5014601022ARTG 190172Altis Single Incision Sling SystemModel/Catalogue Number: 519650SKU Number: 5195601022ARTG 190173
Manufacturer
Coloplast Pty Ltd
1 Event
- Recall of Restorelle DirectFix Anterior, Restorelle DirectFix Posterior, and Altis Single Incision Sling

Manufacturer

Coloplast Pty Ltd

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

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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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