Primary Device ID | M68987165020 |
NIH Device Record Key | f8aa7287-63c0-4fe8-b56d-d27ff1226da1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARMO Classroom Bleeding Control Kit |
Version Model Number | 02 |
Catalog Number | 87-165 |
Company DUNS | 118492643 |
Company Name | Safeguard US Operating, LLC |
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 | true |
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 | false |
OTC Over-The-Counter | true |
Phone | 855-428-6074 |
sales@safeguardmedical.com | |
Phone | 855-428-6074 |
sales@safeguardmedical.com | |
Phone | 855-428-6074 |
sales@safeguardmedical.com | |
Phone | 855-428-6074 |
sales@safeguardmedical.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M68987165020 [Primary] |
OHO | First Aid Kit Without Drug |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-21 |
Device Publish Date | 2025-07-11 |
M68987165010 | This medical trauma kit is designed for emergencies where severe bleeding or other traumatic inj |
M68987165020 | This medical trauma kit is designed for emergencies where severe bleeding or other traumatic inj |