Icu Medical, Inc.

6 product lines across 3 device categories: Angiographic catheters, Implanted ports, Tunneled central lines.

From icumed.com, checked November 2026.

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About Icu Medical, Inc.

Icu Medical, Inc. hasn't added a company description yet.

Angiographic Catheters

Used in: Uterine Artery Embolization (UAE), Internal Iliac Artery Embolization

ProductSizes (FDA GUDID)ModelsMRI
ICU Medical
ANGIOGRAPHIC KIT w/WASTE BAG, LARGE BORE, IV TUBING & ADMIN SET
Length: 150 cm13Not stated
Transpac
Cath Lab Kit /Transpac™ IT and 3ml Flush Device
—4Not stated

Implanted Ports (Port-a-Cath)

Used in: Port-a-Cath (Implanted Port) Placement

ProductSizes (FDA GUDID)ModelsMRI
Deltec
—130MR Conditional
Portex
—1Not stated
ICU Medical, Inc.
GIN for 21-4437-24, POWER PAC, VEN LP, TI, PU, 1.9MM, UL, 6 FR/INTRO, 1/EA
Catheter Gauge: 6 Fr1MR Conditional

Tunneled Central Venous Catheters (Broviac, Hickman)

Used in: Tunneled Central Line (Broviac or Hickman) Placement

ProductSizes (FDA GUDID)ModelsMRI
Deltec
—4Not stated

Sales representatives

Icu Medical, Inc. has not listed representatives here yet. Contact the company directly:

From icumed.com, checked November 2026.

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Frequently asked questions

What devices does Icu Medical, Inc. make?

Icu Medical, Inc. has 6 product lines in our library across 3 device categories: Angiographic catheters, Implanted ports, Tunneled central lines.

How do I contact a Icu Medical, Inc. sales representative?

Icu Medical, Inc. has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.

Does LA Vascular sell Icu Medical, Inc. products?

No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Icu Medical, Inc. or its representatives to buy.

Where do the Icu Medical, Inc. product sizes come from?

From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.

Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.

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