Devices

Device Recall Hemofiltration Standard Pack including BC 60 PlusT 8036

Model / Serial
Lot/batch number: 3000001571 UDI code: 607567206489
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Distributed to the states of NM, CA, and IL.
Product Description
Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. || Used in extracorporeal circulation during cardiopulmonary bypass procedures lasting 6 hours or less.
Manufacturer
Maquet
1 Event
- Recall of Device Recall Hemofiltration Standard Pack including BC 60 PlusT 8036

Manufacturer

Maquet

Manufacturer Address
Maquet, 15 Law Dr, Fairfield NJ 07004-3206
Manufacturer Parent Company (2017)
Getinge AB
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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