DEVICE: MARK 5 NUVO LITE (00038214001421)

Device Identifier (DI) Information

MARK 5 NUVO LITE
525NFD
In Commercial Distribution
525NFD
NIDEK MEDICAL PRODUCTS, INC.
00038214001421
GS1

1
161382940 *Terms of Use
115V OCSI OXYGEN CONCENTRATOR -- FLOW ALARM DEACTIVATED
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
No
Yes
No
No
No
No

GMDN

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
Stationary oxygen concentrator A stationary mains electricity (AC-powered) device designed to concentrate oxygen (O2) from ambient air and deliver the concentrated O2, typically through an attached nasal cannula, to a patient requiring oxygen therapy. It processes the air through an internal filtration system, e.g., a molecular sieve (zeolite granules or membranes), having a large total surface area to separate nitrogen (N2) from the air. It typically consists of an air compressor, filters, dual chambers, a reservoir and controls. The O2 concentration is variable depending on the flow rate utilized. It is typically wheeled but is designed to be placed in one location, e.g., an institution or a home setting.
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FDA Product Code

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Product Code Product Code Name
CAW Generator, Oxygen, Portable
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K123738 000
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Sterilization

No
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

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Storage and Handling
Storage Environment Temperature: between -20 and 60 Degrees Celsius
Storage Environment Humidity: between 15 and 95 Percent (%) Relative Humidity
Storage Environment Atmospheric Pressure: between 64 and 101 KiloPascal
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Clinically Relevant Size

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Size Type Text
No Device Sizes
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Device Record Status

e11d7a96-c5d0-47a7-b1fc-75d66e849e28
July 06, 2018
3
August 23, 2016
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Alternative and Additional Identifiers Additional Identifiers

Package DI

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Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

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Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

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Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
Yes
No
Yes
No CLOSE

Customer Contact

[?]
800-822-9255
info@nidekmedical.com
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