Primary Device ID | 10858778006345 |
NIH Device Record Key | ddd4f881-6cba-4f6a-bc09-8c486db9d5db |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | S1UVC-6540 |
Company DUNS | 791238046 |
Company Name | FOOTPRINT MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 2102262600 |
info@footprintmed.com |
Catheter Gauge | 6.5 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858778006348 [Primary] |
GS1 | 10858778006345 [Package] Contains: 00858778006348 Package: Carton [5 Units] In Commercial Distribution |
FOS | Catheter, Umbilical Artery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-20 |
00858778006850 - N/A | 2024-04-05 Umbilical Probe |
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