Devices

Device Recall APS 1

Model / Serial
Serial numbers 0020 through 0216.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide-USA, Australia, Belgium, Canada, China, Dominican Republic, Egypt, Germany, India, Indonesia, Japan, Malaysia, Mexico, Pakistan, Republic of China, Singapore, South Africa, South Korea, Thailand and United Arab Emirates.
Product Description
Terumo Advanced Perfusion System 1 Integrated Centrifugal System Control Unit; Catalog No. 801046.
Manufacturer
Terumo Cardiovascular Systems Corp
1 Event
- Recall of Device Recall APS 1

Manufacturer

Terumo Cardiovascular Systems Corp

Manufacturer Address
Terumo Cardiovascular Systems Corp, 6200 Jackson Rd, Ann Arbor MI 48103-9586
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall APS 1

Model / Serial
Serial numbers 0033 through 1263.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide-USA, Australia, Belgium, Canada, China, Dominican Republic, Egypt, Germany, India, Indonesia, Japan, Malaysia, Mexico, Pakistan, Republic of China, Singapore, South Africa, South Korea, Thailand and United Arab Emirates.
Product Description
Terumo Advanced Perfusion System 1 Roller Pump 6 inch diameter; Catalog No. 801041.
Manufacturer
Terumo Cardiovascular Systems Corp

Device Recall APS 1

Model / Serial
Serial numbers 0031 through 1025.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide-USA, Australia, Belgium, Canada, China, Dominican Republic, Egypt, Germany, India, Indonesia, Japan, Malaysia, Mexico, Pakistan, Republic of China, Singapore, South Africa, South Korea, Thailand and United Arab Emirates.
Product Description
Terumo Advanced Perfusion System 1 Roller Pump 4 inch diameter; Catalog No. 801040.
Manufacturer
Terumo Cardiovascular Systems 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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