Devices

Device Recall Boston Scientific HTA Thermal endometrial ablation system

Model / Serial
Unit Numbers: IN0350JG, IN0351JG,
Product Classification
Obstetrical and Gynecological Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide-USA, UK, Denmark, Italy, and France
Product Description
HTA Console System, 230 Volt , French, Product Number: 56001FO (HTA system is a software-controlled hysteroscopic thermal endometrial ablation system)
Manufacturer
Boston Scientific Corporation
1 Event
- Recall of Device Recall Boston Scientific HTA Thermal endometrial ablation system

Manufacturer

Boston Scientific Corporation

Manufacturer Address
Boston Scientific Corporation, One Boston Scientific Place, Natick MA 01760-1536
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall Boston Scientific HTA Thermal endometrial ablation system

Model / Serial
Unit Numbers: IN0335JC, IN0337JC, IN0341JD, IN0342JD, IN0343JD, IN0344JE, IN0345JE, IN0347JE, IN0348JE, IN0349JE, IN0352JG, IN0353JG, IN0355JG, IN0356JG
Product Classification
Obstetrical and Gynecological Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide-USA, UK, Denmark, Italy, and France
Product Description
HTA Console System, 230 Volt, English, Product Number: 560010 (HTA system is a software-controlled hysteroscopic thermal endometrial ablation system)
Manufacturer
Boston Scientific Corporation

Device Recall Boston Scientific HTA Thermal endometrial ablation system

Model / Serial
Unit Numbers: IN0339JC, IN0340JC,
Product Classification
Obstetrical and Gynecological Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide-USA, UK, Denmark, Italy, and France
Product Description
HTA Console System, 230 Volt , Italian, || Product Number: 56001 IO (HTA system is a software-controlled hysteroscopic thermal endometrial ablation system)
Manufacturer
Boston Scientific Corporation

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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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