Primary Device ID | 00026072011010 |
NIH Device Record Key | a1209da7-cf45-4e7c-8e67-e8d148d80318 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lifogen |
Version Model Number | 0022-230P |
Catalog Number | 31-01-0600 |
Company DUNS | 099674145 |
Company Name | ALLIED HEALTHCARE PRODUCTS, 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 | true |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00026072011010 [Primary] |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-08 |
Device Publish Date | 2016-09-20 |
00260720012114 | Kit, Soft-Case |
00260720011018 | Emergency Oxygen Unit |
00026072011010 | Emergency Oxygen Unit |
00026072012116 | Kit, Soft-Case |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIFOGEN 97908649 not registered Live/Pending |
MOLAVI SALMAN 2023-04-26 |