FilmQA Pro 987957

GUDID 00810106410845

Radiation/Radiology Software

ASHLAND SPECIALTY INGREDIENTS G.P.

Radiation therapy software

• Primary Device ID: 00810106410845
• NIH Device Record Key: 5abfb0f2-26e9-409f-a861-d36a983b8b3a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FilmQA Pro
• Version Model Number: 8.0
• Catalog Number: 987957
• Company DUNS: 152728887
• Company Name: ASHLAND SPECIALTY INGREDIENTS G.P.
• 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	00810106410845 [Primary]

FDA Product Code

• MWW: Accessory - Film Dosimetry System

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: 2025-02-20
• Device Publish Date: 2025-02-12

On-Brand Devices [FilmQA Pro]

• 00850000065000: 7.0
• 00810106410845: Radiation/Radiology Software