IBO surgical Ratchet Wrench for controlled torque application during Implant placement and prosthetic fixation. Designed for use with the IBO Conical REACTIVE line and matched-platform prosthetic components. Reference ACMC43, Ratchet Wrench Long ACMC43, supplied as a reusable surgical instrument.
Used during Implant placement and prosthetic seating to apply controlled torque per the manufacturer's loading protocol. Final torque values must be applied per IBO's loading specification for the matched Implant or abutment and per the practitioner's clinical judgement based on bone quality and prosthetic plan.
Compatible with IBO Conical REACTIVE platforms (Ø3.0, NP Ø3.5, RP Ø4.3, WP Ø5.0) when paired with the matched-platform Driver / torque adapter from the IBO instrument set. Consult the IBO surgical kit reference for specific Driver pairings.
| Manufacturer reference | ACMC43 |
|---|---|
| Brand | IBO |
| Product family | Surgical Ratchet Wrench |
| Designation | Ratchet Wrench Long ACMC43 |
| Material | Surgical titanium alloy / Ti-6Al-4V ELI |
| Reusable | Yes — autoclave-compatible per IFU |
| Compatibility | IBO Conical REACTIVE Ø3.0 / NP / RP / WP via matched drivers |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
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.
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.
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.