Cerner Patient Observer - CERNER CORPORATION

Duns Number:042410688

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More Product Details

Catalog Number

CFG_PATOBSRVR

Brand Name

Cerner Patient Observer

Version/Model Number

CPO-SP

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

KMI

Product Code Name

Monitor, Bed Patient

Device Record Status

Public Device Record Key

62eb37ce-3da1-42c4-aa87-de5f29d54674

Public Version Date

October 08, 2019

Public Version Number

1

DI Record Publish Date

September 30, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CERNER CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 6
2 A medical device with a moderate to high risk that requires special controls. 19