PathNet® Blood Bank Transfusion

GUDID 00853023006173

CERNER CORPORATION

Blood bank information system application software

• Primary Device ID: 00853023006173
• NIH Device Record Key: 458bed95-fb68-460d-bb3c-f4da94387076
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PathNet® Blood Bank Transfusion
• Version Model Number: PathNet Blood Bank Transfusion 2018
• Company DUNS: 042410688
• Company Name: CERNER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	00853023006173 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK990007

FDA Product Code

• MMH: Blood Establishment Computer Software And Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-05-08

On-Brand Devices [PathNet® Blood Bank Transfusion]

• 00853023006173: PathNet Blood Bank Transfusion 2018
• 00853023006098: PathNet Blood Bank Transfusion 2012
• 00853023006067: PathNet Blood Bank Transfusion2015