Tenderfoot Toddler Heel Stick Device TFT50I

GUDID 20711234303082

Tenderfoot Toddler Heel Stick Device 50/box

ACCRIVA DIAGNOSTICS HOLDINGS, INC.

Blood lancet, single-use
Primary Device ID20711234303082
NIH Device Record Keyf541a3af-2bc3-4b85-8f62-b81ee6bc7fb5
Commercial Distribution StatusIn Commercial Distribution
Brand NameTenderfoot Toddler Heel Stick Device
Version Model NumberTFT50I
Catalog NumberTFT50I
Company DUNS079299318
Company NameACCRIVA DIAGNOSTICS HOLDINGS, INC.
Device Count50
DM Exempttrue
Pre-market Exemptfalse
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

Phone1-800-643-1640
EmailUDI@accriva.com
Phone1-800-643-1640
EmailUDI@accriva.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com
Phone1-800-678-0710
Emaililsd_ra.na@werfen.com

Device Dimensions

Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter
Length3 Millimeter
Depth2 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100711234303088 [Unit of Use]
GS120711234303082 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
JCADevice, Bleeding Time

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-11-19
Device Publish Date2016-09-22

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