Carpentier

GUDID 20643169490134

Cardiopulmonary bypass cannula, femoral Cardiopulmonary bypass cannula, femoral

Primary Device ID	20643169490134
NIH Device Record Key	d88fedb7-c4e6-4a91-b0fc-3a797088bc95
Commercial Distribution Status	In Commercial Distribution
Brand Name	Carpentier
Version Model Number	58733
Company DUNS	006261481
Company Name	MEDTRONIC, INC.
Device Count	4
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Size Text, specify	0
Device Size Text, specify	0

Device Issuing Agency	Device ID
GS1	00643169490130 [Unit of Use]
GS1	20643169490134 [Primary]

DWF	CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Steralize Prior To Use	false
Device Is Sterile	true