RESPOND Exhalation Manifold 91-101-US501

GUDID 00850057117394

CORVENT MEDICAL, INC

Transport electric ventilator
Primary Device ID00850057117394
NIH Device Record Key41898c06-93c2-429a-a140-e96c10e92434
Commercial Distribution StatusIn Commercial Distribution
Brand NameRESPOND Exhalation Manifold
Version Model NumberRESPOND Exhalation Manifold
Catalog Number91-101-US501
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100850057117394 [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 Date2026-01-14
Device Publish Date2026-01-06

On-Brand Devices [RESPOND Exhalation Manifold]

00850057117349RESPOND Exhalation Manifold
00850057117394RESPOND Exhalation Manifold

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