Hood, Capnography Pedo, Unscented 12 Pk 43037-9

GUDID 00813830026061

ACCUTRON, INC.

Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use Anaesthesia face mask, single-use
Primary Device ID00813830026061
NIH Device Record Keya2c9cbb4-21f5-4e46-8e5c-7f69f9e382a5
Commercial Distribution StatusIn Commercial Distribution
Brand NameHood, Capnography Pedo, Unscented 12 Pk
Version Model Number43037-9
Catalog Number43037-9
Company DUNS088302096
Company NameACCUTRON, 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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100813830026061 [Primary]

FDA Product Code

KHAMask, Scavenging

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-27

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