Primary Device ID | 10841470111721 |
NIH Device Record Key | 9eaa9bd7-61b2-445e-9738-308b03a6c775 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | O2-MAX |
Version Model Number | 313-8003XN |
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 | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841470111724 [Primary] |
GS1 | 10841470111721 [Package] Contains: 00841470111724 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 | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2018-10-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
O2-MAX 90533721 not registered Live/Pending |
Engineered Medical Systems, Inc. 2021-02-18 |