International Medical Devices Database

Manufacturer Parent Company (2017)
Device Consulting Pty Ltd
Source
DHTGA
2 Events
- Recall of Laser Guide, Endotherapy, single use - TXMF600BFS Fibres, when using pullback device
- Recall of miraDry System (used for the treatment of primary axillary hyperhidrosis)

2 devices in the database

Laser Guide, Endotherapy, single use - TXMF600BFS Fibres, when using pullback device

Model / Serial
Laser Guide, Endotherapy, single use - TXMF600BFS Fibres, when using pullback deviceBatch Numbers: 1606018 and 1607019ARTG Number: 221756

miraDry System (used for the treatment of primary axillary hyperhidrosis)

Model / Serial
miraDry System (used for the treatment of primary axillary hyperhidrosis)All batches affectedARTG Number: 223967

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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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Device Consulting Pty Ltd

2 devices in the database

Laser Guide, Endotherapy, single use - TXMF600BFS Fibres, when using pullback device

miraDry System (used for the treatment of primary axillary hyperhidrosis)