406503

GUDID 05415067042873

Cardiovascular catheter sheath

Primary Device ID	05415067042873
NIH Device Record Key	db020430-104d-4e9b-8146-7572673af0f4
Commercial Distribution Status	In Commercial Distribution
Version Model Number	406503
Catalog Number	406503
Company DUNS	149818952
Company Name	ST. JUDE MEDICAL, INC.
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	false
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

Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area
Special Storage Condition, Specify	Between 0 and 0 *Store in a dark and dry area

Device Issuing Agency	Device ID
GS1	05414734030052 [Previous]
GS1	05415067042873 [Primary]

DQR	CANNULA, CATHETER

Steralize Prior To Use	false
Device Is Sterile	true