Sale price$218.87

Special Order Item

Est. Delivery:
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Description

  • WARNING: Cancer and Reproductive Harm -

Product Specs

Item Number 504102
Catalog Number CS-50
UOM CS
Level 1 Family Description Nursing and Surgical Supplies
Level 2 Category Description IV Therapy
Level 3 Group Description Other IV Therapy
Level 4 Sub-Category Description Dispenser Iv Fluid, Parenteral
Application Spike, IV Access
Buy American Act (BAA) Compliant No
Country of Origin Mexico
Latex Free Indicator Not Made with Natural Rubber Latex
Manufacturer ICU Medical
Manufacturer # CS-50
McKesson # 504102
Specifications Clave Multidose
Trade Agreement Act (TAA) Compliant Yes
UNSPSC Code 42221612

Frequently asked questions

Is this device safe for patients with latex allergies?

Yes, the ICU Medical Spike is specifically engineered without natural rubber latex, making it a safe choice for both patients and clinical staff who have latex sensitivities.

Can this be used in government or federal facilities?

Yes, this product is fully TAA (Trade Agreement Act) compliant, meaning it meets the necessary procurement standards for facilities requiring regulated supplies.

Is this product compatible with Clave protocols?

Yes, the spike features the Clave multidose specification, ensuring it is designed for reliable and consistent performance within standard IV therapy protocols.

Is this considered a professional-grade medical device?

Absolutely. It is manufactured by ICU Medical, a trusted and reputable leader in medical supplies, and is engineered specifically for clinical fluid therapy and parenteral dispensing.

Is this a sterile, single-use product?

Yes, the ICU Medical Spike is a sterile, single-use component intended to maintain hygiene standards in clinical settings.

Are there specific ordering requirements to be aware of?

Please note that this is a Special Order Item with a lead time of approximately 2-3 weeks. Plan your procurement schedule accordingly to ensure inventory availability.

Does this require specific handling for insertion?

The spike is designed with a sturdy grip flange, which provides a distinct stop point during insertion, and features lateral barbs or “wings” to ensure the spike remains securely anchored within the fluid container.

Is this made in the USA?

While it is TAA compliant, this specific device is manufactured in Mexico.

Why is there a Prop 65 warning on this item?

The WARNING: Cancer and Reproductive Harm notice is a standard disclosure provided for medical-grade plastic instruments as required by regulatory guidelines regarding material components.

What is the catalog number for reference?

The model/catalog number for this specific unit is CS-50.