MasteRad MasteRad MX30

GUDID 00860001404753

MasteRad MX-30 Radiographic System

Medicatech Usa, Inc.

Stationary basic diagnostic x-ray system, digital

• Primary Device ID: 00860001404753
• NIH Device Record Key: d0388759-f30e-4d2e-bd1b-bf2d49a82d3b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MasteRad
• Version Model Number: MasteRad MX30
• Catalog Number: MasteRad MX30
• Company DUNS: 008468677
• Company Name: Medicatech Usa, 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com
• Phone: +1 949-679-2881
• Email: info@medicatechusa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860001404753 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190601

FDA Product Code

• KPR: System, X-Ray, Stationary

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-30
• Device Publish Date: 2024-12-20