mediCAD®

GUDID 04260489720110

mediCAD Hectec GmbH

Orthopaedic/craniofacial implantation planning software

• Primary Device ID: 04260489720110
• NIH Device Record Key: 8f3dd2d2-33e7-4734-b4ac-269ba5dcff88
• Commercial Distribution Discontinuation: 2027-04-16
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mediCAD®
• Version Model Number: 7
• Company DUNS: 328565361
• Company Name: mediCAD Hectec GmbH
• Device Count: 1
• DM Exempt: true
• 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: false
• Manufacturing Date: false
• 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: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu
• Phone: +498713302030
• Email: info@medicad.eu

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260489720110 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170702

FDA Product Code

• LLZ: System, Image Processing, Radiological

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: 2025-04-24
• Device Publish Date: 2025-04-16