Cerner Patient Observer CFG_PATOBSRVR

GUDID 00853023006197

CERNER CORPORATION

Inpatient motion surveillance software
Primary Device ID00853023006197
NIH Device Record Key62eb37ce-3da1-42c4-aa87-de5f29d54674
Commercial Distribution StatusIn Commercial Distribution
Brand NameCerner Patient Observer
Version Model NumberCPO-SP
Catalog NumberCFG_PATOBSRVR
Company DUNS042410688
Company NameCERNER CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100853023006197 [Primary]

FDA Product Code

KMIMonitor, Bed Patient

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-10-08
Device Publish Date2019-09-30

On-Brand Devices [Cerner Patient Observer]

00853023006234CPO-SP6
00853023006203CPO-SP4
00853023006197CPO-SP
00853023006241CPO-I415
00850017753037CPO-SP7

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