Primary Device ID | 00850057117141 |
NIH Device Record Key | 844e7ce6-f5e3-432a-aad8-2a9f48f6dfa8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Removeable Battery |
Version Model Number | Removeable Battery |
Catalog Number | 91-101-US301 |
Company DUNS | 117496308 |
Company Name | CORVENT MEDICAL, 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 | false |
Lot Batch | false |
Serial Number | true |
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 |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com | |
Phone | (833)770-8368 |
support@corventmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850057117141 [Primary] |
CBK | Ventilator, Continuous, Facility Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-31 |
Device Publish Date | 2024-12-23 |