CATHETER 038442 PF 5PK 6F ANGIO KIT Medical Device Identification

GUDID 20613994941941

Angiographic catheter, single-use Angiographic catheter, single-use

Primary Device ID	20613994941941
NIH Device Record Key	15294f8d-75da-4b95-9045-b854eaa485ac
Commercial Distribution Status	In Commercial Distribution
Version Model Number	038442
Company DUNS	006261481
Company Name	MEDTRONIC, 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	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Catheter Gauge	6 French
Catheter Gauge	6 French

Special Storage Condition, Specify	Between 0 and 0 *Store catheters in a cool, dry area.
Special Storage Condition, Specify	Between 0 and 0 *Store catheters in a cool, dry area.

Device Issuing Agency	Device ID
GS1	00613994941947 [Primary]
GS1	20613994941941 [Package] Contains: 00613994941947 Package: PK [5 Units] In Commercial Distribution

DQO	CATHETER, INTRAVASCULAR, DIAGNOSTIC

Steralize Prior To Use	false
Device Is Sterile	true