IBO - Closed Tray Impression Copyng + Screw - INTHEX NP (3.5mm) NP. Inox - # HEI-35710
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Description
Closed Tray Imp HEI-35710
DESCRIPTION
IBO Closed-Tray Impression Coping for conventional Impression workflows, reference HEI-35710, Closed Tray Imp HEI-35710. Used with a standard (non-perforated, Closed) Impression Tray; the Coping remains on the implant when the Tray is removed and is then transferred to the Impression for analog mounting in the laboratory.
CLINICAL APPLICATION
Used at the Impression visit in conventional analog workflows for single-implant or simple cases where a fully passive multi-unit master model is not required. The Coping is screwed onto the implant, the Closed-Tray Impression is taken, the Tray is removed leaving the Coping in the mouth, the Coping is then unscrewed and re-seated into the Impression material for laboratory analog mounting.
PLATFORM & COMPATIBILITY
Used with IBO implant platforms per the MFG# prefix (HEI / HEC / HE). Confirm platform pairing via the IBO catalogue.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HEI-35710 |
|---|---|
| Brand | IBO |
| Product family | Closed-Tray Impression Coping |
| Designation | Closed Tray Imp HEI-35710 |
| Workflow | Conventional / analog Closed-Tray Transfer-pin Impression |
| Material | Ti-6Al-4V ELI Grade 5 |
| Compatibility | IBO Conical Reactive + multiunit platforms — per MFG# prefix |
| 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.