DUCOR 534597T

GUDID 20705032014103

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

Primary Device ID	20705032014103
NIH Device Record Key	6106fff9-50cd-46f8-860b-5c67b93c6bbd
Commercial Distribution Status	In Commercial Distribution
Brand Name	DUCOR
Version Model Number	534597T
Catalog Number	534597T
Company DUNS	806136177
Company Name	CORDIS CORPORATION
Device Count	10
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
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

Device Issuing Agency	Device ID
GS1	10705032014106 [Unit of Use]
GS1	20705032014103 [Primary]

DQO	CATHETER, INTRAVASCULAR, DIAGNOSTIC

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
DUCOR 72241982 0825371 Dead/Cancelled	CORDIS CORPORATION 1966-03-28