DRX Plus 3543 Detector AC2600

GUDID 60889974000221

AY-PACKED-3543 DETECTOR-DRX PLUS

CARESTREAM HEALTH, INC.

Indirect flat panel x-ray detector Indirect flat panel x-ray detector

• Primary Device ID: 60889974000221
• NIH Device Record Key: cadad768-5a4d-4110-8ee2-491460cf2df8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRX Plus 3543 Detector
• Version Model Number: DRX Plus 3543 Detector
• Catalog Number: AC2600
• Company DUNS: 793169512
• Company Name: CARESTREAM HEALTH, 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: true
• 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	60889974000221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150766

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: 5
• Public Version Date: 2019-05-07
• Device Publish Date: 2016-09-16

On-Brand Devices [DRX Plus 3543 Detector]

• 60889974000221: AY-PACKED-3543 DETECTOR-DRX PLUS
• 60889975950532: PACKED, 3543 DETECTOR, DRX PLUS