Device Recall ActiveCare SFT

Model / Serial
Device Catalog Number A502B-0001-01 and A502B-0002-01
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
ActiveCare +SFT || Medical Compression Systems || OR Aqiva, IL || Intended for use in: Preventing deep Vein Thrombosis; Enhancing blood circulation; Diminishing post-operative pain and swelling; Reducing wound healing time; treatment and assistance in healing of stasis dermatitis, venous stasis ulcers and diabetic leg ulcers; Treatment of chronic venous insufficiency and; Reducing edema
Manufacturer
Medical Compression Systems
1 Event
- Recall of Device Recall ActiveCare SFT

Manufacturer

Medical Compression Systems

Manufacturer Address
Medical Compression Systems, 2 Hallan St, OR Aqiva Israel
Manufacturer Parent Company (2017)
Medical Compression Systems (DBN) Ltd.
Source
USFDA

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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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