AcuityPDR

GUDID 00810035220362

Portable basic diagnostic x-ray system, digital

Primary Device ID	00810035220362
NIH Device Record Key	627a4e97-2c53-4e21-a3c7-529618b2ecdd
Commercial Distribution Status	In Commercial Distribution
Brand Name	AcuityPDR
Version Model Number	Standard
Company DUNS	005057263
Company Name	RADMEDIX, LLC
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	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00810035220362 [Primary]

IZL	System, X-Ray, Mobile

Steralize Prior To Use	true
Device Is Sterile	false

[00810035220362]

Liquid Chemical

[00810035220362]

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[00810035220362]

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[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical

[00810035220362]

Liquid Chemical