Primary Device ID | 00845174009172 |
NIH Device Record Key | b368c1f2-514e-48d1-a1ea-5b809a54a61e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GM |
Version Model Number | 5145GM |
Company DUNS | 944953959 |
Company Name | LIFELINE FIRST AID, 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 | false |
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 | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com | |
Phone | 5037833720 |
qamanager@lifelinefirstaid.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845174009165 [Primary] |
GS1 | 00845174009172 [Package] Contains: 00845174009165 Package: Master [6 Units] In Commercial Distribution |
LRR | First Aid Kit With 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 | 2024-09-11 |
Device Publish Date | 2024-09-03 |
00845174009196 | SAFETY OCCUPANT KIT |
00845174009172 | GM EMERGENCY ROAD KIT |
00845174009158 | CADILLAC CREST HSK-ELEC |
00845174009134 | CADILLAC CREST HIGHWAY EMERGENCY KIT |