N/A

GUDID 00858778006850

Umbilical Probe

FOOTPRINT MEDICAL, INC.

Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use Abdominal/ENT/orthopaedic surgical probe, single-use
Primary Device ID00858778006850
NIH Device Record Key35ccb251-2b03-48a4-a70d-1f52e24be806
Commercial Distribution StatusIn Commercial Distribution
Brand NameN/A
Version Model NumberPROBE-UMB
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 Latexfalse
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
GS100858778006850 [Primary]
GS110858778006857 [Package]
Package: Box [25 Units]
In Commercial Distribution

FDA Product Code

KDCInstrument, Surgical, Disposable

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-05
Device Publish Date2024-03-28

Devices Manufactured by FOOTPRINT MEDICAL, INC.

00858778006850 - N/A2024-04-05Umbilical Probe
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