GUDID 00858778006843

Fenestrated Drape with Clear Window

FOOTPRINT MEDICAL, INC.

Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use
Primary Device ID00858778006843
NIH Device Record Key35868fd5-0d88-4b75-98c1-277004c0d604
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberMAXDRAPE
Company DUNS791238046
Company NameFOOTPRINT MEDICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com
Phone2102262600
Emailinfo@footprintmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100858778006843 [Primary]
GS110858778006840 [Package]
Package: Box [15 Units]
In Commercial Distribution

FDA Product Code

PUIDrape, Surgical, Exempt

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-06
Device Publish Date2022-09-28

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