UDI-DI variants

208 UDI-DI variants

No registered UDI-DI variants for this device family.

Data from EUDAMED, last updated May 23, 2026

Straight rod, Rod, Commercially Pure Rod, Commercially Pure Rod with Hex Ends, Dual Diameter Rod, Dual Diameter Straight Rod, etc.

0705034a0016667

208 UDI-DI variants

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

Implantable

Basic UDI-DI: 0705034a0016667
Device name: Straight rod, Rod, Commercially Pure Rod, Commercially Pure Rod with Hex Ends, Dual Diameter Rod, Dual Diameter Straight Rod, etc.
Device model: EXPEDIUM Spine System Rod
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 18, 2026

208 UDI-DI variants

No registered UDI-DI variants for this device family.