Saudi Arabia SFDA registration ME0000000283SFDAA00278
A-V Impulse
Saudi Arabia·Medical Device·Covidien llc·Class IIActiveProduct information
Intermittent Compression system
Product use
The A-V Impulse System is indicated circulation enhancement, deep vein thrombosis (DVT) and pulmonary embolism prophylaxis, acute and chronic oedema, leg pain incident to trauma or surgery, leg ulcers, venous stasis and insufficiency, and lymphoedema.
Device classification
- Risk Class
- Class II
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000283SFDAA00278
- Authorization ID
- GHTF-2017-0090
- Status
- Active
- Expire Date
- April 20, 2020
Manufacturer
- Manufacturer Name
- Covidien llc
Model information
- Model ID(s)
- AV6000-AUS AV6000-EUR AV6060-USA AV6000-UK
Product accessories
[{'tradeName': 'AV Impulse Impad Rigid Sole Foot Cover', 'description': None, 'gmdn': ''}]
About this record
Access comprehensive regulatory information for A-V Impulse in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000000283SFDAA00278 and manufactured by Covidien llc.
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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