Stryker Neurovascular | TransForm™ Occlusion Balloon Catheter

The TransForm Occlusion Balloon Catheter is a single-lumen occlusion balloon for use with endovascular coil embolization.

Features and benefits

Fast inflate and deflate

Synchro™ Guidewire technology along the length of the balloon provides fast deflation, allowing for higher contrast levels, increased visibility, and reduced procedure times.

Smooth trackability

The delivery wire has four different material transition zones for excellent balance between proximal pushability and distal flexibility.

Increased stability

TransForm Occlusion Balloon Catheter is 0.14in guidewire compatible. Designed to provide controlled balloon inflation, quick wall apposition, and stability.

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Specifications

TransForm Compliant

Balloon nominal diameter	Balloon nominal length
3mm	10mm
3mm	15mm
4mm	10mm
4mm	15mm
4mm	20mm
4mm	30mm
5mm	10mm
5mm	15mm
5mm	20mm
5mm	30mm

TransForm Super Compliant

Balloon nominal diameter	Balloon nominal length
3mm	5mm
4mm	7mm
4mm	10mm
7mm	7mm
7mm	10mm
7mm	15mm

Compatibility

Balloon catheter type	Effective length	Max catheter shaft OD	Min guide catheter ID	Recommended guidewire in OD
Compliant	150cm	2.8F (0.95mm)	0.053in (1.35mm)	Stryker Neurovascular 0.014in (0.36mm)
Super Compliant	150cm	2.8F (0.95mm)	0.053in (1.35mm)	Stryker Neurovascular 0.014in (0.36mm)

Additional resources

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

DFU excerpt

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.