DEPUY CODMAN MODC18854

GUDID 20886704044137

Angiographic catheter, single-use

Primary Device ID	20886704044137
NIH Device Record Key	dc7bc4a5-0371-4933-99fa-22dab418f403
Commercial Distribution Status	In Commercial Distribution
Brand Name	DEPUY CODMAN
Version Model Number	MODC18854
Catalog Number	MODC18854
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

Special Storage Condition, Specify	Between 0 and 0 *To prevent damage to the catheter tip during removal from the package, grasp the hub and withdraw the catheter
Special Storage Condition, Specify	Between 0 and 0 *Exposure to temperatures above 54 degrees C (130 F) may damage the catheter
Special Storage Condition, Specify	Between 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, Specify	Between 0 and 0 *Do not use if package is opened or damaged
Special Storage Condition, Specify	Between 0 and 0 *To prevent damage to the catheter tip during removal from the package, grasp the hub and withdraw the catheter
Special Storage Condition, Specify	Between 0 and 0 *Exposure to temperatures above 54 degrees C (130 F) may damage the catheter
Special Storage Condition, Specify	Between 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, Specify	Between 0 and 0 *Do not use if package is opened or damaged

Device Issuing Agency	Device ID
GS1	20886704044137 [Primary]

DQO	CATHETER, INTRAVASCULAR, DIAGNOSTIC

Steralize Prior To Use	false
Device Is Sterile	true