Removeable Battery 91-101-US301

GUDID 00850057117141

CORVENT MEDICAL, INC

Transport electric ventilator
Primary Device ID00850057117141
NIH Device Record Key844e7ce6-f5e3-432a-aad8-2a9f48f6dfa8
Commercial Distribution StatusIn Commercial Distribution
Brand NameRemoveable Battery
Version Model NumberRemoveable Battery
Catalog Number91-101-US301
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100850057117141 [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 Date2024-12-31
Device Publish Date2024-12-23

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