ADx Guidewire

GUDID 15051684019019

Peripheral vascular guidewire, manual

Primary Device ID	15051684019019
NIH Device Record Key	77d2a1e2-a5c5-4284-85bd-c55794f9c9f4
Commercial Distribution Status	In Commercial Distribution
Brand Name	ADx Guidewire
Version Model Number	810138260
Company DUNS	079252781
Company Name	Angiodynamics, 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	true
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

Phone	+1(800)772-6446
Email	customerservice@angiodynamics.com
Phone	+1(800)772-6446
Email	customerservice@angiodynamics.com
Phone	+1(800)772-6446
Email	customerservice@angiodynamics.com
Phone	+1(800)772-6446
Email	customerservice@angiodynamics.com

Device Issuing Agency	Device ID
GS1	15051684019019 [Primary]
HIBCC	H7878101382600 [Previous]

DQX	Wire, guide, catheter

Steralize Prior To Use	false
Device Is Sterile	true