interWORKS

GUDID 00850054590046

Avreo Inc

Radiological PACS software

• Primary Device ID: 00850054590046
• NIH Device Record Key: 70d50320-78b2-4a08-b846-21215f86434f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: interWORKS
• Version Model Number: 8.6.0.20824
• 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	00850054590046 [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: 2024-03-19
• Device Publish Date: 2024-03-11

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
• 00850054590107: Version 8.7.0.21176
• 00850054590114: Version 8.7.0.21126
• 00850054590121: Version 8.8.0.21349
• 00850054590138: Version 8.6.0.21481
• 00850054590145: Version 8.9.0.21572
• 00850054590152: Version 8.5.0.21589