DR 10e C XF6RR

GUDID 05414904252529

DR Detector

AGFA

Indirect flat panel x-ray detector

• Primary Device ID: 05414904252529
• NIH Device Record Key: ca1071d0-c9b1-4161-a165-5e86f723d5e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DR 10e C
• Version Model Number: 6011/111
• Catalog Number: XF6RR
• 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 Dimensions

• Length: 24 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	05414904252529 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172784

FDA Product Code

• MQB: Solid state x-ray imager (flat panel/digital imager)

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: 2019-05-07
• Device Publish Date: 2019-04-05

Devices Manufactured by AGFA

• 05414904271124 - SE Suite: 2023-10-18 Software
• 05414904208168 - NX 3.0: 2023-07-26
• 05414904233320 - NX 4.0: 2023-07-26
• 05414904281321 - DR 400: 2023-03-31
• 05414904225066 - Mamoray HDR-C Plus: 2022-11-24
• 05414904231678 - Dentus M2 Comfort: 2022-11-24
• 05414904231692 - Dentus M2 Comfort: 2022-11-24
• 05414904231531 - Dentus Ortholux Register: 2022-11-14