GUDID 10858778006529

PICC Catheter Trimming Device

FOOTPRINT MEDICAL, INC.

Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter
Primary Device ID10858778006529
NIH Device Record Key6ae4e23c-2231-4bfc-97f2-8aef9b391fbc
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberTRIMMER
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

Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com
Phone210-226-2600
Emailinfo@footprintmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100858778006522 [Primary]
GS110858778006529 [Package]
Contains: 00858778006522
Package: Carton [10 Units]
In Commercial Distribution

FDA Product Code

FZTCutter, Surgical

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 Date2016-09-20

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