Primary Device ID | 07540195025066 |
NIH Device Record Key | 4e36fbb2-b380-4aeb-8731-e8458dcdfa26 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CAREvent EMT |
Version Model Number | 01CV1112 |
Catalog Number | 01CV1112 |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800387-3405 |
cs@otwo.com |
Storage Environment Temperature | Between -40 Degrees Celsius and 60 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07540195025066 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-26 |
07540195025066 | The CAREvent EMT kit contains a CAREvent EMT resuscitator, a pressure regulator and an aspirator |
07540195025059 | The CAREvent EMT kit contains a CAREvent EMT resuscitator and a pressure regulator in moulded ca |
07540195025042 | CAREvent EMT hand held automatic resuscitator is pneumatically powered, time/volume cycled venti |