Devices

Device Recall Septal occluder

Model / Serial
OEM Catalog number 9-AVP2-012.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Product Description
Medical Device Exchange 12MM VASCULAR; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 9-AVP2-012; || EXP (repackager), Aga Medical (OEM) || Transcatheter septal occluder
Manufacturer
EXP Pharmaceutical Services Corp
1 Event
- Recall of Device Recall Septal occluder

Manufacturer

EXP Pharmaceutical Services Corp

Manufacturer Address
EXP Pharmaceutical Services Corp, 48021Warm Springs Boulevard, Fremont CA 94539
Manufacturer Parent Company (2017)
Abry Partners Inc.
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Septal occluder

Model / Serial
OEM Catalog number 9-AVP2-010.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Product Description
Medical Device Exchange 10MM VASCULAR; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 9-AVP2-010; || EXP (repackager), Aga Medical (OEM) || Transcatheter septal occluder
Manufacturer
EXP Pharmaceutical Services Corp

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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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