GUDID 10858778006826

Silicone Tourniquet

FOOTPRINT MEDICAL, INC.

Arm/leg tourniquet, single-use Limb tourniquet, manual, single-use Limb tourniquet, manual, single-use Limb tourniquet, manual, single-use Limb tourniquet, manual, single-use Limb tourniquet, manual, single-use Limb tourniquet, manual, single-use Limb tourniquet, manual, single-use
Primary Device ID10858778006826
NIH Device Record Keyb927d377-ce16-478b-9428-1554e4d17f04
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberST-S
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 Perscriptionfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100858778006829 [Primary]
GS110858778006826 [Package]
Contains: 00858778006829
Package: Carton [50 Units]
In Commercial Distribution

FDA Product Code

GAXTourniquet, Nonpneumatic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-04-19

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