Primary Device ID | 07540195055032 |
NIH Device Record Key | e5e1b27a-39c9-46a8-a472-62546d1be119 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rescue Breather CPR Protective Barrier |
Version Model Number | 01RB2010-RED-U |
Catalog Number | 01RB2010-R |
Company DUNS | 206449154 |
Company Name | O-Two Medical Technologies 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800-387-3405 |
cs@otwo.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07540195055032 [Primary] |
GS1 | 17540195055039 [Package] Package: Packaging Box [50 Units] In Commercial Distribution |
LYM | Device, Cpr Assist |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2016-09-23 |
17540195055077 | The Rescue Breather consists of a one-way valve that has a large block is placed in a patient's |
17540195055060 | The Rescue Breather consists of a one-way valve that has a large block is placed in a patient's |
07540195055056 | The Rescue Breather consists of a one-way valve that has a large block is placed in a patient's |
17540195055046 | The Rescue Breather consists of a one-way valve that has a large block is placed in a patient's |
07540195055032 | The Rescue Breather consists of a one-way valve that has a large block is placed in a patient's |
07540195055025 | The Rescue Breather consists of a one-way valve that has a large block is placed in a patient's |