Cerner Patient Observer CFG_PATOBSRVR

GUDID 00850017753037

CERNER CORPORATION

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• Primary Device ID: 00850017753037
• NIH Device Record Key: 5f3630c8-0087-4990-9488-8fb410b95dfd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cerner Patient Observer
• Version Model Number: CPO-SP7
• Catalog Number: CFG_PATOBSRVR
• Company DUNS: 042410688
• Company Name: CERNER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850017753037 [Primary]

FDA Product Code

• KMI: Monitor, Bed Patient

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-22
• Device Publish Date: 2020-12-14

On-Brand Devices [Cerner Patient Observer]

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