Primary Device ID | 10841470100145 |
NIH Device Record Key | 7bcb70d9-5f93-480b-bc47-8b4641305428 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | O2-MAX |
Version Model Number | 313-8201-6 |
Company DUNS | 030619483 |
Company Name | PULMODYNE 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841470100148 [Primary] |
GS1 | 10841470100145 [Package] Contains: 00841470100148 Package: [10 Units] In Commercial Distribution |
BYE | Attachment, Breathing, Positive End Expiratory Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-21 |
Device Publish Date | 2025-04-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() O2-MAX 90533721 not registered Live/Pending |
Engineered Medical Systems, Inc. 2021-02-18 |