Primary Device ID | 20711234303082 |
NIH Device Record Key | f541a3af-2bc3-4b85-8f62-b81ee6bc7fb5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tenderfoot Toddler Heel Stick Device |
Version Model Number | TFT50I |
Catalog Number | TFT50I |
Company DUNS | 079299318 |
Company Name | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
Device Count | 50 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800-643-1640 |
UDI@accriva.com | |
Phone | 1-800-643-1640 |
UDI@accriva.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com | |
Phone | 1-800-678-0710 |
ilsd_ra.na@werfen.com |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Length | 3 Millimeter |
Depth | 2 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00711234303088 [Unit of Use] |
GS1 | 20711234303082 [Primary] |
FMK | Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature |
JCA | Device, Bleeding Time |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-19 |
Device Publish Date | 2016-09-22 |
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