EVOBITE SPA00200

GUDID 08050038830065

3DIEMME SRL

Dental guided surgery registration/navigation fiducial marker

• Primary Device ID: 08050038830065
• NIH Device Record Key: 8a55b917-7d2d-49e8-8070-e0ebe6271d1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVOBITE
• Version Model Number: EVOFLAT
• Catalog Number: SPA00200
• Company DUNS: 857172105
• Company Name: 3DIEMME SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08050038830065 [Primary]

FDA Product Code

• EHY: Tray, Impression, Preformed

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: 2023-02-14
• Device Publish Date: 2023-02-06

Devices Manufactured by 3DIEMME SRL

• 08050038833226 - RealGUIDE Z3D KIT, Empty Tray: 2026-03-18
• 08050038834407 - RealGUIDE Z3D Surgical Kit: 2026-03-18
• 18050038834411 - RealGUIDE Sleeve: 2026-03-18
• 18050038834428 - RealGUIDE Sleeve: 2026-03-18
• 18050038834435 - RealGUIDE Sleeve: 2026-03-18
• 18050038834442 - RealGUIDE Sleeve: 2026-03-18
• 18050038834459 - RealGUIDE Sleeve: 2026-03-18
• 18050038834466 - RealGUIDE Sleeve: 2026-03-18