Product Specifications
|
Parameter |
Specification |
|
Housing Configuration |
Split-shell handle and enclosure set for reusable or single-use laparoscopic instruments |
|
Material Options |
Medical-grade PC, ABS, or PC/ABS; heat-sterilizable engineering resin for reusable versions |
|
Shaft Interface Range |
5–12 mm |
|
Critical Interface Tolerance |
±0.05 mm at pivots, shaft seats, bosses, and shell mating features |
|
Nominal Wall Thickness |
1.2–3.5 mm |
|
Sterilization Configuration |
Autoclave-compatible version up to 134°C |
|
Chemical Resistance |
Alcohol and glutaraldehyde cleaning solutions |
|
Grip Surface |
Anti-slip texture, soft-grip overmolding, or germ-resistant additive |
|
Insert Options |
Metal pins, threaded inserts, and shaft-interface components |
|
Assembly Methods |
Snap fit, screw fastening, or ultrasonic welding |
|
Supply Condition |
Non-sterile molded parts or assembled housing sets |
Key Advantages
● Accurate Alignment Of Internal Mechanisms
Molded bosses, bearing seats, trigger pivots, shaft interfaces, and cable channels share one tolerance system. Correct alignment helps the trigger or knob move repeatedly without binding, uneven loading, or added stress on the internal mechanism.
● Grip Geometry For Gloved Operation
Handle contour, finger clearance, texture, and optional soft overmolding are developed for the intended hand position. The grip remains controllable in wet or gloved use without requiring excessive hand force.
● Material Selection For The Intended Reprocessing Method
Housing resin is selected for the specified disinfectant, sterilization cycle, temperature, and number of uses. The chosen material and wall structure limit cracking, warpage, and surface degradation under repeated cleaning or the validated single-use process.




Customization Options
● Housing Interfaces
Shell geometry, shaft connection, and trigger-mounting positions are developed from the supplied device design.
● Material And Grip
Resin, surface texture, and any soft-grip area are matched to the intended handling and reprocessing method.
● Inserts And Assembly
The manufacturing scope can include metal inserts or pins and the approved screw, snap, or welding method.
Customization Process
Device Definition
Confirm the internal mechanism, shaft interface, and reprocessing method.
DFM Review
Finalize pivot locations, boss structure, and the critical tolerance stack.
Tooling Development
Build the housing mold and any required insert fixtures.
T1 Functional Fit
Verify shell closure, trigger movement, and shaft alignment with the supplied mechanism.
Pilot Approval
Confirm critical dimensions, assembly performance, and the approved molding conditions.
Manufacturing Handover
Release the approved mold, assembly method, and reference sample to routine production.
Quality Control
● Material And Insert Traceability
Resin and metal inserts are checked by grade and lot before molding or assembly.
● Functional Dimension Control
Trigger pivots, shaft alignment, and shell mating surfaces are measured to the control plan.
● Assembly And Surface Check
Sample assemblies are checked for free movement and proper closure. Visible surfaces receive a final inspection afterward.
FAQ
Q1: What order quantity applies to a new Laparoscope Housing?
A1: The normal MOQ is one standard container. The quantity is converted into housing sets according to the approved component combination and packing plan.
Q2: Which shipping terms are available for Laparoscope Housing orders?
A2: Available shipping terms are EXW, FOB, and CIF. The quotation and order confirmation state the selected term, loading point, documentation scope, and freight responsibility.
Q3: Is every Laparoscope Housing suitable for autoclaving?
A3: No. Autoclave compatibility depends on the resin, wall design, assembly method, temperature, pressure, and cycle count. Validation must use the complete device and its specified sterilization process.
Q4: Are the housings supplied sterile?
A4: Standard supply is non-sterile molded or assembled components. Sterilization and sterile-barrier packaging require a separate validated specification and supply arrangement.
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