International Medical Devices Database

Manufacturer Address
Danatech Medical Systems Inc, 7275 Nw 68th St Ste 1, Miami FL 33166-3094
Source
USFDA
1 Event
- Recall of Device Recall Sonotrax

One device in the database

Device Recall Sonotrax

Model / Serial
Product is uncoded.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed to 89 consumers nationwide.
Product Description
Product is a handheld fetal Doppler used to screen for fetal heart rate and averaged fetal heart rate and is labeled as: Sonotrax Handheld Fetal Doppler Series and includes the Basic and Lite models.

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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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Danatech Medical Systems Inc

One device in the database

Device Recall Sonotrax