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PEAK SURGICAL
SKU:PS-1113
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The Single Use Malis Bayonet Bipolar Forceps 21.6cm are specialized electrosurgical forceps designed for controlled bipolar coagulation during operative procedures. The Malis-style bayonet configuration offsets the working end from the handle axis, providing a dedicated instrument profile for surgical fields where direct access and visibility around the distal tips are important.
The current Peak Surgicals model is identified as SKU PS-1113. The listed size is 8½ inches (21.6 cm), and the current product specification identifies German stainless steel construction.
This Peak Surgicals configuration has a listed overall size of 8½ inches (21.6 cm). The extended length provides working reach while maintaining manual control from the proximal forceps body.
The 21.6 cm size is an important purchasing identifier when distinguishing this model from other Malis-style bipolar forceps available in different overall lengths.
The instrument uses a Malis-style bayonet configuration. In a bayonet forceps design, the working section is offset from the main handle axis rather than remaining completely straight.
This geometry is commonly selected when a surgeon requires a clearer working line around the distal portion of the instrument. The exact offset dimensions and working length of this Peak Surgicals model are not stated on the current product page.
The current Peak Surgicals listing classifies PS-1113 as Bipolar Forceps within its electrosurgical instrument range. Bipolar forceps are used with an appropriate electrosurgical system to deliver current between the two forceps tips for controlled tissue coagulation.
The exact generator settings, compatible electrosurgical units, connector standard, cable requirements, and electrical specifications are not provided on the current product page. These should be confirmed before use with a specific electrosurgical system.
Peak Surgicals' electrosurgical instrument range identifies bipolar forceps for coagulating tissue using electrical current. The forceps therefore provide both a mechanical gripping interface and paired bipolar electrodes at the working end.
Energy settings and application technique should be determined by the appropriately trained surgeon according to the tissue, procedure, and compatible electrosurgical generator being used.
The current product specification lists German stainless steel as the material for PS-1113. The metallic construction provides the structural form required for the forceps body and working ends.
The exact stainless-steel alloy grade is not stated on the current Peak Surgicals page. Hospitals and procurement teams requiring a specific steel grade or material certificate should confirm that specification before ordering.
The current Peak Surgicals specification lists Operating Room among the usage environments for the Malis Bayonet Bipolar Forceps. The instrument is positioned within the company's Single Use Bipolar Forceps and broader electrosurgical instrument ranges.
The current page does not assign PS-1113 to one specific surgical specialty, so procedure-specific claims beyond its bipolar electrosurgical function should not be assumed.
The current Peak Surgicals page does not provide an exact tip width, tip angle, working length, insulation specification, or stop configuration for PS-1113.
Malis-style bipolar forceps from other manufacturers are produced in multiple tip widths and configurations, but those specifications should not be transferred to this Peak Surgicals model without direct confirmation.
Before ordering, buyers should confirm compatibility with the intended bipolar electrosurgical system. The live Peak Surgicals page does not state a specific generator manufacturer, plug configuration, cable model, or universal compatibility standard.
Compatibility should therefore be verified according to the electrosurgical unit and accessories used by the healthcare facility.
The product is currently named and categorized by Peak Surgicals as Single Use Malis Bayonet Bipolar Forceps. However, the same live specification table also contains reusable wording.
For procurement accuracy, the intended single-use or reusable status should be confirmed from the final product specification and labeling before clinical use.
| Product Name | Single Use Malis Bayonet Bipolar Forceps |
| SKU / Model Number | PS-1113 |
| Instrument Type | Bipolar Forceps |
| Pattern | Malis Bayonet |
| Listed Size | 8½ Inches / 21.6 cm |
| Material | German Stainless Steel |
| Primary Function | Bipolar Electrosurgical Tissue Coagulation |
| Listed Usage | Operating Room / Professional Surgical Use |
| Product Range | Single Use Bipolar Forceps / Electrosurgical Instruments |
| Exact Tip Width | Not Specified on Current Product Page |
| Working Length | Not Specified on Current Product Page |
| Non-Stick Coating | Not Confirmed for This Product |
| Cable / Connector Compatibility | Not Specified on Current Product Page |
The Single Use Malis Bayonet Bipolar Forceps are relevant for hospitals, operating rooms, surgical centers, electrosurgical instrument distributors, and procurement teams sourcing Malis-pattern bipolar forceps.
For accurate purchasing, buyers can reference SKU PS-1113 together with the 8½-inch (21.6 cm) size, Malis bayonet pattern, and German stainless-steel construction. Exact tip width, insulation, working length, cable or connector configuration, generator compatibility, and confirmed single-use status should be verified before ordering.
They are bipolar electrosurgical forceps designed for controlled tissue coagulation during appropriate operative procedures.
The current Peak Surgicals listing identifies the size as 8½ inches (21.6 cm).
The current Peak Surgicals model number is PS-1113.
The current product specification lists German stainless steel. The exact steel alloy grade is not stated.
The current Peak Surgicals page does not identify PS-1113 as a non-stick model, so a non-stick coating should not be assumed.
The product name and collection classify them as Single Use, while the current specification table also states “Reusable.” This conflicting product data should be confirmed and corrected before final clinical or procurement use.
