reNEW™ Certified Pre-Owned System NA

GUDID 00811376030351

Linear accelerator system

Primary Device ID	00811376030351
NIH Device Record Key	e3b4a2a6-3ba3-4d60-92f5-3ba3cbd2e11c
Commercial Distribution Status	In Commercial Distribution
Brand Name	reNEW™ Certified Pre-Owned System
Version Model Number	H-0000-0003
Catalog Number	NA
Company DUNS	080044624
Company Name	Accuray Incorporated
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	false
Lot Batch	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
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	00811376030351 [Primary]
HIBCC	M65810466130 [Previous]

IYE	Accelerator, Linear, Medical

Steralize Prior To Use	false
Device Is Sterile	false

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