Removeable Batt. Chrg, 4-slot, 30% Max Charge 91-101-US315

GUDID 00850057117288

CORVENT MEDICAL, INC

Transport electric ventilator
Primary Device ID00850057117288
NIH Device Record Key443fa4bc-7be5-45f9-807e-4f7628959316
Commercial Distribution StatusIn Commercial Distribution
Brand NameRemoveable Batt. Chrg, 4-slot, 30% Max Charge
Version Model NumberRemoveable Batt. Chrg, 4-slot, 30% Max Charge
Catalog Number91-101-US315
Company DUNS117496308
Company NameCORVENT MEDICAL, INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com
Phone(833)770-8368
Emailsupport@corventmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850057117288 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CBKVentilator, Continuous, Facility Use

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-06-13
Device Publish Date2025-06-05

Devices Manufactured by CORVENT MEDICAL, INC

00850057117370 - RESPOND Ventilator2026-01-14
00850057117387 - Flow Sensor2026-01-14
00850057117394 - RESPOND Exhalation Manifold2026-01-14
00850057117400 - Exhalation Valve2026-01-14
00850057117417 - RESPOND HME Patient Circuit Kit (Tubing, Connector & HME/2026-01-14
00850057117424 - HEPA Filters2026-01-14
00850057117448 - Green Oxygen Hose, 8ft2026-01-14
00850057117455 - Oxygen Tubing with Connector, 7ft2026-01-14

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.