Primary Device ID | 10858778006826 |
NIH Device Record Key | b927d377-ce16-478b-9428-1554e4d17f04 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | ST-S |
Company DUNS | 791238046 |
Company Name | FOOTPRINT MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com | |
Phone | 2102262600 |
info@footprintmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858778006829 [Primary] |
GS1 | 10858778006826 [Package] Contains: 00858778006829 Package: Carton [50 Units] In Commercial Distribution |
GAX | Tourniquet, Nonpneumatic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-04-19 |
00858778006850 - N/A | 2024-04-05 Umbilical Probe |
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10859950007501 - NA | 2022-10-07 Polyurethane Feeding Tube with male Enteral Connector 5.0Fr by 60cm |
10859950007518 - NA | 2022-10-07 Polyurethane Feeding Tube with male Enteral Connector 6.5Fr by 60cm |