Cardioplegia Cannula

GUDID 38033178017191

Cardioplegia cannula

Primary Device ID	38033178017191
NIH Device Record Key	30a345bc-79fd-491d-b16d-c9a714284f2a
Commercial Distribution Status	In Commercial Distribution
Brand Name	Cardioplegia Cannula
Version Model Number	AR-11012
Company DUNS	442126587
Company Name	SORIN GROUP ITALIA SRL
Device Count	1
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	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	08033178017190 [Primary]
GS1	38033178017191 [Package] Contains: 08033178017190 Package: CASE [10 Units] In Commercial Distribution

DWF	Catheter, cannula and tubing, vascular, cardiopulmonary bypass

Steralize Prior To Use	false
Device Is Sterile	true