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Sapphire II PRO 1.0

Balloon Dilatation Catheter

Cross with Confidence
Every Time

Single Material Tip

The small size Sapphire II PRO has a single-material tip for a simpler construction. The shorter tip facilitate better tracking. And the low tip entry profile is engineered for very tight lesions

Tip entry profile

The single material tip enables the lowest entry profile for excellent crossability in very tight lesions

Lubricious Coating

Hydro-X Hydrophilic coating on distal shaft for added crossability

Hydro-X hydrophilic coating is a water-absorbing, very slippery coating that reduces friction during lesion crossing

IMPROVES CROSSABILITY

Invio hydrophobic coating is a water-repelling, slippery coating that reduces guidewire friction

IMPROVES TRACKABILITY

G-70-1126 Rev01

CSI is a registered trademark belonging to Cardiovascular Systems, Inc.

Technical Specifications Available Configurations Product Downloads

Technical Specifications

Proximal Shaft Diameter	1.9F
Distal Shaft Diameter	2.36F
Leading Tip Length	1.5 mm
Balloon Material	Nylon
Balloon Pleats	2 folds (ø1.0 mm); 3 folds (ø1.25 mm & 1.5 mm)
Compliance	Semi-compliant
Tip Entry Profile	0.0164” (ø1.0 mm)
Marker Bands	1 marker
Coating	Hydrophilic (distal tip to guidewire exit marker); Hydrophobic (guidewire lumen)
Crossing Profile	0.0216” (ø1.0 mm)
Nominal Pressure	6 atm
Rated Burst Pressure	14 atm

Compliance Chart

Pressure (atm)	Balloon Diameter (Ø mm)
	1.0	1.25	1.5
2	0.83	1.04	1.29
4	0.94	1.17	1.42
6 NOM*	1.00	1.25	1.5
8	1.04	1.30	1.56
10	1.08	1.35	1.60
12	1.11	1.38	1.63
14 RBP**	1.13	1.41	1.66
16	1.15	1.44	1.69
18	1.17	1.46	1.71

* Nominal Pressure. The nominal in vitro device specifications do not take into account any lesion resistance.
**Rated Burst Pressure. Do not exceed RBP

G-70-1127 Rev01

Available Configurations

Balloon Diameter (Ø mm)	Balloon Working Length (mm)
	5	8	10	12	15	20	30
1.0	●	●	●	–	●	–	–
1.25	●	●	●	–	●	–	–
1.5	–	–	●	●	●	●	–

G-70-1128-01

G-70-1125 Rev03 Sapphire 2 PRO Brochure_FDA Approved

G-70-1129 Rev02

Sapphire® II PRO is cleared for sale in the USA. Caution: Federal Law (US) restricts this device to sale by or on order of a physician.