interWORKS

GUDID 00850054590091

Avreo Inc

Radiological PACS software

• Primary Device ID: 00850054590091
• NIH Device Record Key: 074c6c40-56bb-4883-93b3-5e30ef775c9b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: interWORKS
• Version Model Number: Version 8.7.0.21082
• Company DUNS: 175766216
• Company Name: Avreo Inc
• 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	00850054590091 [Primary]

FDA Product Code

• LMD: System, Digital Image Communications, Radiological

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: 2024-11-19
• Device Publish Date: 2024-11-11

On-Brand Devices [interWORKS]

• 00850054590015: 8.5.20356
• 00850054590022: 8.5.20530
• 00850054590039: 8.5.0.20530
• 00850054590046: 8.6.0.20824
• 00850054590053: Version 8.6.0.20860
• 00850054590060: Version 8.6.0.20917
• 00850054590077: Version 8.6.0.20992
• 00850054590084: Version 8.6.0.21040
• 00850054590091: Version 8.7.0.21082