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The Excelsior SL-10 Microcatheter is designed with thin-wall technology and lubricious Hydrolene™ outer surface

Features and benefits

Image of 1.7F (0.60mm) Low profile distal shaft

1.7F (0.60mm) Low profile distal shaft

Excelsior SL-10 Microcatheter is designed with a low profile tip to enhance access to distal vasculature.

Atraumatic distal tip

Specifically engineered for atraumatic access, the rounded, low-durometer, unbraided tip offers softness and flexibility

Image of Variety of tip shapes

Variety of tip shapes

Offered in six clinically relevant shapes to improve access and navigability

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Product specifications

Specifications

Excelsior SL-10 Microcatheters 

Description  Total / Distal length  Proximal / Distal OD Proximal / Distal ID
Straight, 2-tip marker 150cm/6.0cm 2.4F/1.7F 0.79mm/0.56mm 0.0165in/0.0165in 0.42mm/0.42mm
Pre-Shaped 45, 2-tip marker 150cm/6.0cm
Pre-Shaped 90, 2-tip marker 150cm/6.0cm
Pre-Shaped J, 2-tip marker 150cm/6.0cm
Pre-Shaped C, 2-tip marker 150cm/6.0cm
Pre-Shaped S, 2-tip marker 150cm/6.0cm
Straight, 1-tip marker 150cm/6.0cm
Compatibility
Effective length Max catheter shaft OD Min catheter shaft OD Proximal / Distal ID Recommended guidewire OD
150cm 2.4F (0.80mm) 1.7F (0.60mm) 0.0165in (0.42mm) Stryker Neurovascular 0.014in (0.36mm)

Additional resources

Looking for more information about this product? Please contact your local sales representative.

DFU excerpt

Pre-shaped microcatheter DFU. See package insert for complete indications, complications, warnings, and instructions for use. (Uploaded on 21/5/2018.)

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SL-10 microcatheter DFU. See package insert for complete indications, complications, warnings, and instructions for use. (Uploaded on 21/5/2018.)

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  • THIS CONTENT IS INTENDED SOLELY FOR THE USE OF HEALTHCARE PROFESSIONALS. A physician must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that physicians be trained in the use of any particular product before using it in a procedure. The information presented is intended to demonstrate the breadth of Stryker product offerings. A physician must always refer to the package insert, product label and/or instructions for use before using any Stryker product. Products may not be available in all markets because product availability is subject to the regulatory and/ or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area. The Stryker products listed above are CE marked according to the Medical Device Directive 93/42/EEC.
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