Lifogen 31-01-0600
GUDID 00260720011018
Emergency Oxygen Unit
ALLIED HEALTHCARE PRODUCTS, INC.
Fixed-regulator oxygen cylinder| Primary Device ID | 00260720011018 |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00260720011018 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K895956
FDA Product Code
| CAN | Regulator, Pressure, Gas Cylinder |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-20 |
On-Brand Devices [Lifogen]
| 00260720012114 | Kit, Soft-Case |
| 00260720011018 | Emergency Oxygen Unit |
| 00026072011010 | Emergency Oxygen Unit |
| 00026072012116 | Kit, Soft-Case |
Trademark Results [Lifogen]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LIFOGEN 97908649 not registered Live/Pending |
MOLAVI SALMAN 2023-04-26 |
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