Ultra PC % Flowmeter, EU Model 31975-EU

GUDID 00813830025385

Medical gas mixer

ACCUTRON, INC.

Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Inhalational analgesia unit Oxygen/air/nitrous oxide breathing gas mixer Oxygen/air/nitrous oxide breathing gas mixer
Primary Device ID00813830025385
NIH Device Record Key06dfc188-e7ad-44a4-9f54-83faaf306452
Commercial Distribution Discontinuation2199-04-18
Commercial Distribution StatusIn Commercial Distribution
Brand NameUltra PC % Flowmeter, EU Model
Version Model Number31975-EU
Catalog Number31975-EU
Company DUNS088302096
Company NameACCUTRON, INC.
Device Count1
DM Exempttrue
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 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
GS100813830025385 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BSZGas-Machine, Anesthesia

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-27
Device Publish Date2023-04-19

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