Venti.Plus Hyperinflation System 1.0L

GUDID 44710810117396

GALEMED CORPORATION

Anaesthesia face mask, reusable
Primary Device ID44710810117396
NIH Device Record Key450f69e2-6197-4609-b47e-e47725e6ff5c
Commercial Distribution StatusIn Commercial Distribution
Brand NameVenti.Plus
Version Model NumberH100
Catalog NumberHyperinflation System 1.0L
Company DUNS656854379
Company NameGALEMED CORPORATION
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104710810117398 [Primary]
GS144710810117396 [Package]
Contains: 04710810117398
Package: Carton [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHKResuscitator,Manual,Non Self-Inflating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-24

On-Brand Devices [Venti.Plus]

44710810117396H100
44710810117389H050
44710810117372H025
44710810100503H100-M
44710810100497H050-M
44710810100480H025-M

Trademark Results [Venti.Plus]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VENTI.PLUS
VENTI.PLUS
77881643 not registered Dead/Abandoned
GALEMED CORPORATION
2009-11-28
VENTI.PLUS
VENTI.PLUS
77645179 not registered Dead/Abandoned
GALEMED CORPORATION
2009-01-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.