Medical device licence · 60439 · Class 2
CARDIOVASCULAR PROCEDURE KIT
Yes: licensed in Canada
Licence status Issued (active); first licensed September 10, 2002. It is in Health Canada’s list of active licences.
- Licence number
- 60439
- Licence holder
- Terumo Cardiovascular Systems CorporationTustin, CA, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group Family
- First licensed
- September 10, 2002
- Devices covered
- 23
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- CARDIOPULMONARY BYPASS MACHINE PROC. WITH X-COATED HEART-LUNG PERFUSION KIT
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT (ADULT HOSPITAL PACK)
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT (ADULT PERFUSION PACK)
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT (H-L PACK)
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH A-V SET
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH BLOOD SPIKE
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH CONNECTOR
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH CONNECTOR AND TUBING
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH DOUBLE RAPID PRIME
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH HEMOCONCENTRATOR KIT
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH LUER CONNECTOR
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH MALE SWIVEL CONNECTOR
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH O2 GAS LINE TUBING
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH PERFUSION ADAPTER
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH PRESSURE MONITORING LINE
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH PUMP AND TABLE PACK
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH QUICK PRIME LINE
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH SILICONE U TUBE
- CARDIOPULMONARY BYPASS MACHINE PROCEDURE KIT WITH Y CONNECTOR
- CARDIOVASCULAR PROCEDURE KIT (AFO2X KIT)
- CARDIOVASCULAR PROCEDURE KIT (X-COATED VENOUS SEQUESTRATION)
- CARDIOVASCULAR PROCEDURE KIT: M/F EXTENSION LINE
- CARDIOVASCULAR PROCEDURE KIT: VAVD KIT
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.