SUPERTORQUE PLUS 533532

GUDID 20705032012543

Angiographic catheter, single-use

Primary Device ID	20705032012543
NIH Device Record Key	92d0c250-1999-4759-b936-5e88771d984d
Commercial Distribution Status	In Commercial Distribution
Brand Name	SUPERTORQUE PLUS
Version Model Number	533532
Catalog Number	533532
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	10705032012546 [Primary]
GS1	20705032012543 [Package] Contains: 10705032012546 Package: Box [5 Units] In Commercial Distribution

DQO	Catheter, intravascular, diagnostic

Steralize Prior To Use	false
Device Is Sterile	true