IBO - Non-Engaging Temporary Abutment height 1.5mm Gold Anodised - INTHEX NP (3.5mm) NP. Titanium - # HEI-35611
Description
Non-Engaging Multiunit Component — HEI-35611
DESCRIPTION
IBO Non-Engaging multiunit-platform component, reference HEI-35611, Non-Engaging HEI-35611. Designed for multi-implant prosthetic workflows where rotational latitude is required for passive-fit splinted restorations on non-parallel implants.
CLINICAL APPLICATION
Used in multi-implant prosthetic workflows where the rotational lock of an engaging interface would compromise the passive fit of a splinted prosthesis. The Non-Engaging interface allows the prosthetic component to seat without forcing rotational alignment to the implant's anti-rotation feature.
PLATFORM & COMPATIBILITY
Platform pairing per the MFG# prefix — HEI for IBO Internal Hex platforms, HEC for Conical Reactive (Ø3.5 NP / Ø4.3 RP) platforms. Consult the IBO catalogue for the specific implant fixture pairing.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HEI-35611 |
|---|---|
| Brand | IBO |
| Product family | Non-Engaging Multiunit Variant |
| Designation | Non-Engaging HEI-35611 |
| Connection style | Non-Engaging |
| Material | Ti-6Al-4V ELI Grade 5 |
| Compatibility | Per MFG# prefix — HEI / HEC |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
MATERIALS & SURFACE
Machined from medical-grade Ti-6Al-4V ELI Titanium (Grade 5), ASTM F136 / ISO 5832-3, selected for biocompatibility, mechanical strength and chemical stability in the oral environment.
All materials and processes comply with current regulations and are subject to full traceability from raw material to final validation.
STERILIZATION & HANDLING
Supplied in the manufacturer's validated condition for clinical use. Follow the package insert and IBO Instructions for Use for handling, storage and any chairside preparation steps. Do not modify the geometry or surface in any way; doing so compromises both clinical fit and regulatory clearance.
Single-use device. Single patient, single procedure. Discard unused components per local biohazard regulations.
QUALITY ASSURANCE
IBO operates under ISO 13485:2016 quality management for the manufacturing of medical devices, holds the AEMPS Spanish Agency of Medicines and Medical Devices licence, and every IBO component carries the CE marking MDR, assessed by a Notified Body.