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Manufacturers
Maquet
Manufacturer Address
Maquet, 15 Law Dr, Fairfield NJ 07004-3206
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA
1 Event
Recall of Device Recall Hemofiltration Standard Pack including BC 60 PlusT 8036
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One device in the database
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.
252 manufacturers with a similar name
Learn more about the data
here
Maquet (Suzhou) Co., Ltd. || Maquet Gmbh & Co. Kg || Maquet Sas
Manufacturer Parent Company (2017)
Getinge AB
Source
NIDFSINVIMA
Maquet Cardiopulmonary A. G.
Manufacturer Parent Company (2017)
Getinge AB
Source
NIDFSINVIMA
Maquet Cardiopulmonary A. G. || Maquet Cardipulmonary- Medikal T
Manufacturer Parent Company (2017)
Getinge AB
Source
NIDFSINVIMA
Maquet Critical Care AB
Manufacturer Parent Company (2017)
Getinge AB
Source
NIDFSINVIMA
Maquet Critical Care Ab
Manufacturer Parent Company (2017)
Getinge AB
Source
NIDFSINVIMA
247 more
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