6 3 4″ Dale Fem Pop Clamp Medium
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100% Autoclavable & Passivated AISI 420 SteelSKU: SP-99293
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-99293AISI 420 Martensitic

6 3/4″ Dale Fem Pop Clamp Medium

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

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The 6 3/4″ Dale Fem Pop Clamp Medium is a specialized vascular surgical instrument identified by its medium configuration and 6.75-inch overall length. It is designed for consideration in femoral and popliteal vascular procedures where an appropriate vascular clamp is required. Confirm the jaw design, dimensions, and material specifications before ordering.

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The 6 3/4″ Dale Fem Pop Clamp Medium is a specialized surgical instrument associated with femoral and popliteal vascular procedures. Its product name identifies the Dale instrument pattern, a medium configuration, and an overall length of 6.75 inches, approximately 17.1 cm.

Femoral and popliteal vascular surgery involves blood vessels in the thigh and knee region. Instruments selected for these procedures must match the intended surgical technique and vessel-control requirements. The appropriate application of this clamp should be confirmed using the manufacturer's specifications and guidance from qualified surgical professionals.

Medium Configuration

The medium designation distinguishes this model within its product range. However, the exact jaw dimensions, opening capacity, and differences between available sizes are not provided in the product title. Buyers should confirm these details before comparing this instrument with small, large, or alternative clamp models.

Correct sizing is an important part of instrument selection. The chosen clamp should be suitable for the intended anatomy and procedure, with its design and operating characteristics verified before clinical use.

Applications in Vascular Surgery

Femoral and popliteal clamps are associated with vascular procedures involving the femoral and popliteal regions. Depending on its verified design and intended use, a clamp in this category may be selected when temporary vessel control is required.

The instrument should not be assumed suitable for every vascular procedure based on its name alone. Surgical teams should follow the manufacturer's stated indications and established clinical protocols when selecting and using the instrument.

Design and Handling Considerations

The 6.75-inch overall length provides a useful specification for cataloging, procurement, and comparison with other vascular instruments. The medium configuration is another identifying feature that can help purchasing teams distinguish this model from related products.

Before use, inspect the instrument for visible damage, alignment issues, and proper mechanical function. Verify the jaw pattern, clamping characteristics, material grade, and reusable status with the supplier. Cleaning, maintenance, and sterilization must follow the manufacturer's validated instructions.

Procurement and Product Verification

The 6 3/4″ Dale Fem Pop Clamp Medium is intended for evaluation by professional surgical instrument buyers, healthcare facilities, and medical procurement teams. Before placing an order, confirm the manufacturer's reference number, exact jaw measurements, construction material, and applicable quality or regulatory documentation.

Accurate product details help ensure the selected instrument matches the requirements of the intended surgical setting.

Key Features

  • Dale Fem Pop Clamp pattern

  • Overall length of 6 3/4 inches

  • Approximate metric length of 17.1 cm

  • Medium configuration

  • Categorized as a vascular surgical instrument

  • Associated with femoral and popliteal vascular surgery

  • Suitable for professional instrument cataloging and procurement

  • Jaw dimensions and operating characteristics require verification

  • Material specification should be confirmed with the supplier

  • Reprocessing must follow validated manufacturer instructions

Product Specifications

SpecificationDetails
Product NameDale Fem Pop Clamp Medium
Instrument CategoryVascular Surgical Instrument
Overall Length6 3/4 inches
Metric LengthApproximately 17.1 cm
Size / ConfigurationMedium
Jaw DesignConfirm with supplier
Intended Surgical AreaFemoral and popliteal vascular procedures
MaterialConfirm with supplier
Jaw DimensionsConfirm with supplier
Manufacturer Reference / SKUConfirm with supplier
Reusable StatusConfirm with manufacturer
Sterilization CompatibilityFollow manufacturer instructions

Frequently Asked Questions

1. What is a Dale Fem Pop Clamp?

A Dale Fem Pop Clamp is a vascular surgical instrument associated with femoral and popliteal procedures. Its precise function depends on the specific model and manufacturer specifications.

2. What is the length of this Dale Fem Pop Clamp?

The listed overall length is 6 3/4 inches, approximately 17.1 cm.

3. What does Medium mean in the product name?

Medium identifies the model's size configuration. Exact differences in jaw dimensions and opening capacity should be confirmed with the supplier.

4. What procedures may require a fem pop clamp?

Instruments in this category are associated with procedures involving the femoral and popliteal vascular regions. Suitability for a particular procedure must be established by qualified professionals.

5. What material is this clamp made from?

The material grade is not specified in the product title. Contact the supplier to confirm the construction material and available documentation.

6. How do I distinguish this model from other sizes?

Compare the manufacturer's model number, jaw dimensions, opening capacity, and overall length. Do not rely on the size label alone.

7. Is this clamp reusable?

Reusable status is not established by the product name. Verify the manufacturer's instructions for use and approved reprocessing requirements.

8. How should the instrument be cleaned and sterilized?

Follow the manufacturer's validated instructions for cleaning, inspection, maintenance, and sterilization. Confirm compatibility with the facility's reprocessing procedures before use.