UDI-DI variants

7 UDI-DI variants

Data from EUDAMED, last updated May 23, 2026

Obturator, Clear Cannula, Blunt, Reusable, Cannulated, Bone Graft, Screw Guide, Introducer, GRYPHON

0886705a00128KJ

7 UDI-DI variants

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

Reusable

Basic UDI-DI: 0886705a00128KJ
Device name: Obturator, Clear Cannula, Blunt, Reusable, Cannulated, Bone Graft, Screw Guide, Introducer, GRYPHON
Device model: General Orthopedic Use Obturators
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026