8 1 4″ Demos Tibial Artery Clamp
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100% Autoclavable & Passivated AISI 420 SteelSKU: SP-59189
OR & Quality SpecificationsHospital Grade
Steel MetallurgyGerman AISI 420 Martensitic
Sterilization Cycle134°C / 273°F Steam Autoclave
Quality StandardISO 13485:2016 & CE Mark
Optical FinishAnti-Glare Satin Matte
Electrochemical PassivationCSSD Laser Batch Tracking
ClampsSKU: SP-59189AISI 420 Martensitic

8 1/4″ Demos Tibial Artery Clamp

4.9 / 5.0•18 Verified OR Evaluations
$100.00$120.00/ unit

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The 8¼″ Demos Tibial Artery Clamp is a specialized vascular surgical instrument intended for use in procedures involving tibial artery access and control, subject to manufacturer specifications. Its defined overall length helps professionals identify the appropriate instrument for their surgical inventory. Confirm the jaw configuration, clamping mechanism, and material before purchase.

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The 8¼″ Demos Tibial Artery Clamp is a specialized surgical instrument designed for vascular applications involving the tibial artery, according to the manufacturer's intended-use specifications. Its 8¼-inch overall length provides a useful reference for healthcare professionals and purchasing teams comparing vascular clamps for specialized procedures. The Demos designation identifies the instrument style, while the exact jaw design and operating characteristics should be verified with the supplier.

Tibial artery clamps are selected for procedures where controlled vascular clamping is required in the relevant anatomical area. Instrument selection depends on the surgical approach, vessel characteristics, access requirements, and the design of the clamp. The overall length is one consideration, but jaw shape, working length, width, and contact-surface pattern are also important when determining whether a specific instrument is suitable for the intended procedure.

The product title does not specify whether this Demos Tibial Artery Clamp has straight, curved, or angled jaws. It also does not provide jaw dimensions, the clamping surface pattern, or details of the locking mechanism. These features should be confirmed through manufacturer documentation or a technical product image before ordering. Buyers should not assume a particular jaw geometry or tissue-contact performance based on the instrument name alone.

The instrument's construction and mechanical function are important considerations in a professional surgical environment. The material, surface finish, joint design, and handle mechanism can affect maintenance requirements and compatibility with established instrument-processing procedures. Purchasing teams should request the manufacturer's specifications to confirm the construction material and intended clinical application.

Before use, trained personnel should inspect the clamp for proper jaw alignment, smooth movement, secure closure, and visible damage. Corrosion, deformation, stiffness, or irregular operation should be addressed according to facility policy and manufacturer guidance. The instrument should only be used by qualified professionals who understand its intended function and the requirements of the procedure.

Cleaning, disinfection, and sterilization must follow the manufacturer's validated instructions for the exact model. Reprocessing compatibility depends on the instrument's material and construction, so reusable status and autoclave suitability should not be assumed unless explicitly confirmed. Healthcare facilities should also verify applicable regulatory documentation and intended-use information before introducing the clamp into clinical practice.

The 8¼″ Demos Tibial Artery Clamp provides a defined size reference for specialized vascular instrument selection. Confirming the jaw dimensions, geometry, material, and operating mechanism with the supplier helps ensure that the selected model meets the requirements of the intended application.

Key Features

  • Demos-style tibial artery clamp

  • 8¼-inch overall length

  • Intended for specialized vascular applications, subject to manufacturer specifications

  • Designed for procedures involving tibial artery clamping when appropriate

  • Jaw geometry and dimensions should be verified

  • Clamping and locking mechanism details are not specified

  • Material composition and surface finish require supplier confirmation

  • Overall length supports instrument size comparison

  • Inspect jaw alignment and mechanical function before use

  • Follow manufacturer instructions for cleaning and sterilization

  • Verify intended use and regulatory documentation before clinical application

Product Specifications

SpecificationDetails
Product NameDemos Tibial Artery Clamp
Overall Length8¼ inches
Instrument CategoryVascular surgical clamp
Design StyleDemos
Intended ApplicationTibial artery clamping, subject to manufacturer specifications
Jaw ConfigurationNot specified
Jaw DimensionsNot provided
Locking MechanismNot specified
MaterialConfirm with manufacturer
Surface FinishNot specified
Cleaning and SterilizationFollow manufacturer-validated instructions
Model NumberNot provided

Frequently Asked Questions

1. What is an 8¼″ Demos Tibial Artery Clamp used for?

It is a specialized vascular instrument intended for procedures involving tibial artery clamping, subject to the manufacturer's intended-use specifications.

2. What is the overall length of this clamp?

The listed overall length is 8¼ inches.

3. What type of jaws does the Demos Tibial Artery Clamp have?

The product title does not specify the jaw shape. Check the supplier's product image or technical documentation for confirmation.

4. What material is used to manufacture this instrument?

The material is not specified in the title. Contact the manufacturer or supplier for details about the construction material and surface finish.

5. Does this clamp have a locking mechanism?

The locking mechanism is not identified in the supplied title. Verify whether the model includes a ratchet or another closure mechanism.

6. Is this clamp suitable for every tibial artery procedure?

No. Suitability depends on the specific procedure, anatomical requirements, instrument design, and manufacturer specifications. Qualified healthcare professionals should determine its appropriate use.

7. How should the clamp be cleaned and sterilized?

Follow the manufacturer's validated cleaning, disinfection, and sterilization instructions for the exact model. Do not assume compatibility with a particular sterilization method.

8. What should buyers confirm before ordering?

Verify the 8¼-inch length, jaw shape and dimensions, material, locking mechanism, intended application, and reprocessing requirements.