DX-D 600 5R2XP

GUDID 05414904092293

DX-D 600 MANUAL SYSTEM

AGFA

Stationary basic diagnostic x-ray system, digital

• Primary Device ID: 05414904092293
• NIH Device Record Key: 1f2c6fd9-e301-4276-ae09-09dbf63c9508
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DX-D 600
• Version Model Number: 5430/100
• Catalog Number: 5R2XP
• Company DUNS: 374444883
• Company Name: AGFA
• 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: true
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: +1(877)777-2432
• Email: salesinfo@agfa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05414904092293 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112670

FDA Product Code

• KPR: System, x-ray, stationary

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-06-14
• Device Publish Date: 2016-09-01

On-Brand Devices [DX-D 600]

• 05414904108802: DX-D 600 ANALOG MANUAL SYSTEM
• 05414904092316: DX-D 600 AUTOMATIC SYSTEM
• 05414904092309: DX-D 600 SEMI-AUTOMATIC SYSTEM
• 05414904092293: DX-D 600 MANUAL SYSTEM