Devices

Danis Procedure Pack and Danis Procedure Pack - Basic

Model / Serial
Danis Procedure Pack and Danis Procedure Pack - BasicProduct Reference Numbers: 019-08S-25-135 and 019-08S-25-135-BLot Numbers: P14080073-01, P15020247-01, P15030171-01, P15110018-01, P15100210-01 and P17010044-01 ARTG Number: 95573
Manufacturer
Endotherapeutics Pty Ltd
1 Event
- Recall of Danis Procedure Pack and Danis Procedure Pack - Basic

Manufacturer

Endotherapeutics Pty Ltd

Manufacturer Parent Company (2017)
Endotherapeutics Pty. Limited
Source
DHTGA

One device with a similar name

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guide wire being part of the danis procedure pack and danis procedure pack - basic.

Model / Serial
Manufacturer
ELLA-CS

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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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