CirQPOD System

GUDID 00847946028350

CIRQPOD SYSTEM

Zoll Medical Corporation

Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory Cardiopulmonary resuscitation impedance valve, inspiratory
Primary Device ID00847946028350
NIH Device Record Key69ae5329-89ab-4e75-8fd2-7851c62b99f9
Commercial Distribution StatusIn Commercial Distribution
Brand NameCirQPOD System
Version Model Number12-2415-000
Company DUNS055363428
Company NameZoll Medical Corporation
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Operating and Storage Conditions

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Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Handling Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Handling Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment Atmospheric PressureBetween 0 KiloPascal and 0
Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Handling Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment Atmospheric PressureBetween 0 KiloPascal and 0
Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Handling Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment Atmospheric PressureBetween 0 KiloPascal and 0
Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Handling Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment Atmospheric PressureBetween 0 KiloPascal and 0
Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Handling Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
Storage Environment Atmospheric PressureBetween 0 KiloPascal and 0
Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 0 Degrees Celsius
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Storage Environment Atmospheric PressureBetween 0 KiloPascal and 0
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Device Identifiers

Device Issuing AgencyDevice ID
GS100847946028350 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BWFSPIROMETER, THERAPEUTIC (INCENTIVE)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-09
Device Publish Date2020-07-01

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