Cerner Bridge Medical Transfusion Administration and Specimen Collections

GUDID 00853023006104

CERNER CORPORATION

Blood bank information system application software

• Primary Device ID: 00853023006104
• NIH Device Record Key: 82d9a30b-ca3d-41ab-9585-30b191603b78
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cerner Bridge Medical Transfusion Administration and Specimen Collections
• Version Model Number: Bridge2016
• 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	00853023006104 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK060037

FDA Product Code

• MMH: Software, Blood Bank, Stand Alone Products

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: 2016-09-24

Devices Manufactured by CERNER CORPORATION

• 00850017753136 - FetaLink+: 2025-07-11
• 00850017753129 - FetaLink: 2025-04-29
• 00850017753112 - FetaLink+: 2024-06-03
• 00850017753037 - Cerner Patient Observer: 2020-12-22
• 00853023006241 - Cerner Patient Observer: 2020-02-10
• 00853023006197 - Cerner Patient Observer: 2019-10-08
• 00853023006203 - Cerner Patient Observer: 2019-10-08
• 00853023006234 - Cerner Patient Observer: 2019-10-08