DUCOR 534699T

GUDID 10705032014564

Angiographic catheter, single-use

Primary Device ID	10705032014564
NIH Device Record Key	36a0bc34-13d0-465e-ba97-5c0a344d0773
Commercial Distribution Status	In Commercial Distribution
Brand Name	DUCOR
Version Model Number	534699T
Catalog Number	534699T
Company DUNS	806136177
Company Name	CORDIS CORPORATION
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

Device Issuing Agency	Device ID
GS1	10705032014564 [Primary]
GS1	20705032014561 [Package] Package: BOX [10 Units] In Commercial Distribution

DQO	CATHETER, INTRAVASCULAR, DIAGNOSTIC
OEZ	Cardiovascular Procedure Kit

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