Median sternotomy exposure
HK-SR opens and maintains the surgical access required for selected open cardiac procedures.
A cardiac access instrument for median sternotomy exposure. Its primary role is exposure—not tissue stabilization—and its relationship with other AeroMed products should be described as a documented configuration rather than a mandatory chain.
Reprocessing, accessories, documented mounting relationships, and third-party use should follow the current IFU and technical evaluation.
HK-SR opens and maintains the surgical access required for selected open cardiac procedures.
It does not perform local cardiac stabilization or heart positioning.
HK-FXG-Q and selected Heart Stabilizer relationships should be confirmed in the IFU.
Cleaning, inspection, sterilization, and lifecycle control are document-led.
HK-SR provides median sternotomy exposure. It may also form part of a documented AeroMed mounting configuration, but it should not be described as the universal mounting platform for every cardiac product.

Reusable retraction instrument for selected open cardiac surgery workflows.

Detailed dimensions, material, opening range, accessories, and inspection criteria should come from the current technical file.
The source page presents HK-SR with HK-FXG-Q and selected Heart Stabilizer configurations. Exact assembly should be verified before use.
| Parameter | Public Website Description |
|---|---|
| Product name | HK-SR Sternal Retractor |
| Product category | Reusable cardiac surgery access instrument |
| Primary role | Median sternotomy exposure and retraction |
| Material | Reusable stainless-steel construction; detailed information available in technical documentation |
| System integration | Selected HK-FXG-Q and Heart Stabilizer configurations where documented |
| Reprocessing | Cleaning, inspection, and sterilization according to IFU and hospital procedure |
| Manufacturer | Beijing HangTian KaDi Technology R&D Institute |
Provides sternotomy exposure and serves as the structural access instrument.
Presented in the source page as a documented interface for selected AeroMed Heart Stabilizer mounting workflows.
Performs stabilization or positioning and remains a separate device family.
Confirm cleanliness, function, locking, surface condition, and required sterilization according to the IFU.
Follow validated hospital reprocessing steps and compatible sterilization parameters.
Do not publish an unsupported case count. Remove the device from service according to inspection and IFU criteria.
HK-SR is presented as a CE MDR Class I reusable instrument. The page does not make a standalone FDA approval or clearance claim.
HK-SR is a reusable cardiac surgical instrument for median sternotomy exposure. It belongs to the Surgical Exposure group of the AeroMed Cardiac Surgery portfolio.
No. HK-SR provides surgical exposure. The Heart Stabilizer and compatible SF working end are separate products used for cardiac stabilization or positioning.
The source page presents HK-SR with HK-FXG-Q in a documented AeroMed mounting configuration for selected Heart Stabilizer standoffs. Exact assembly and permitted models should be confirmed against the current IFU.
Yes. The page presents HK-SR as a reusable stainless-steel instrument. Cleaning, inspection, sterilization, and retirement criteria should follow the current IFU and hospital reprocessing procedure.
This page does not make a blanket compatibility claim. Third-party use should be evaluated against dimensions, fixation method, load path, and applicable instructions before clinical use.
Qualified partners can request the current CE documentation, declaration, IFU, model information, reprocessing instructions, catalog pages, packaging details, and product images.
Tell us the target market, required dimensions, intended AeroMed configuration, evaluation quantity, and documentation needs.