Fenestrated Drape with Clear Window Medical Device Identification

GUDID 00858778006843

Patient surgical drape, single-use

Primary Device ID	00858778006843
NIH Device Record Key	35868fd5-0d88-4b75-98c1-277004c0d604
Commercial Distribution Status	In Commercial Distribution
Version Model Number	MAXDRAPE
Company DUNS	791238046
Company Name	FOOTPRINT MEDICAL, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00858778006843 [Primary]
GS1	10858778006840 [Package] Package: Box [15 Units] In Commercial Distribution

PUI	Drape, Surgical, Exempt

Steralize Prior To Use	false
Device Is Sterile	true

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