1717 Flat Panel Detector

GUDID 00817100020445

17X17 Flat Panel Detector (GOS)

KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.

Diagnostic x-ray digital imaging conversion system Diagnostic x-ray digital imaging conversion system Diagnostic x-ray digital imaging conversion system

• Primary Device ID: 00817100020445
• NIH Device Record Key: 6d431297-83d5-460c-9fc3-a35477a94103
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1717 Flat Panel Detector
• Version Model Number: PAN252
• Company DUNS: 080269345
• Company Name: KONICA MINOLTA MEDICAL IMAGING U.S.A., 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

Customer Support Contacts

• Phone: 1-800-366-5343
• Email: HTICSupport@konicaminolta.com
• Phone: 1-800-366-5343
• Email: HTICSupport@konicaminolta.com
• Phone: 1-800-366-5343
• Email: HTICSupport@konicaminolta.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817100020445 [Primary]

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: 3
• Public Version Date: 2019-02-21
• Device Publish Date: 2016-09-28

On-Brand Devices [1717 Flat Panel Detector]

• 00817100020452: 17X17 flat Panel Detector (CsI)
• 00817100020445: 17X17 Flat Panel Detector (GOS)