UDI-DI variants

29 UDI-DI variants

No registered UDI-DI variants for this device family.

Data from EUDAMED, last updated May 23, 2026

BioniQ Impression and Laboratory Components

85955730007XW

29 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

No device characteristics flagged

Basic UDI-DI: 85955730007XW
Device name: BioniQ Impression and Laboratory Components
Device model: Closed tray impression post; Pin extension for open tray impression components; Scanbody, BioniQ; ScanPost CEREC; Screw-On closed tray impression coping; Screw-On open tray impression coping; STANDARD impression coping
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 17, 2025

29 UDI-DI variants

No registered UDI-DI variants for this device family.