READYMATIC Developer and Replenisher 5285929

GUDID 60889975285924

READYMATIC DEVELOPER AND REPL, 2X5L

CARESTREAM HEALTH, INC.

X-ray film processing chemical, automatic

• Primary Device ID: 60889975285924
• NIH Device Record Key: 9023d4ad-65f4-4ed9-ae17-7baf3615d12c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: READYMATIC Developer and Replenisher
• Version Model Number: READYMATIC Developer and Replenisher
• Catalog Number: 5285929
• Company DUNS: 793169512
• Company Name: CARESTREAM HEALTH, INC.
• 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: true
• 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	60889975285924 [Primary]

FDA Product Code

• IWZ: Film, radiographic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-08-01

On-Brand Devices [READYMATIC Developer and Replenisher]

• 60889978777532: READYMATIC Developer and Repl - 4x1GL
• 60889975285924: READYMATIC DEVELOPER AND REPL, 2X5L