Serranator Characteristics

Minimum Required Features and Specifications
Salient Characteristics

The requested catheters must meet the following requirements for peripheral vascular interventions. 1. Must have balloon-mounted serration that can provide controlled mechanical lesion modification during peripheral angioplasty. 2. Must be indicated for dilation of peripheral arterial lesions and treatment of obstructive lesions in native or synthetic arteriovenous dialysis fistulae. 3. Must be sterile, disposable, and intended for single use. 4. Must have an over-the-wire catheter design and a 150 cm working length. 5. Must have radiopaque markers identifying the balloon’s working length for positioning under fluoroscopy. 6. Must include manufacturer instructions, balloon compliance information, nominal inflation pressure, and rated burst pressure. 7. Must provide the size and compatibility combinations listed below. Product reference
Balloon diameter × length
Guidewire compatibility
Sheath compatibility

FGS-0682-20040 SL-Pro

2.0 × 40 mm

0.014 inch

5 Fr

FGS-0682-20120 SL-Pro

2.0 × 120 mm

0.014 inch

5 Fr

FGS-0346-25120

2.5 × 120 mm

0.014 inch

6 Fr

FGS-0346-30040

3.0 × 40 mm

0.014 inch

6 Fr

FGS-0346-30120

3.0 × 120 mm

0.014 inch

6 Fr

FGS-0346-35040

3.5 × 40 mm

0.014 inch

6 Fr

FGS-0492-40040

4.0 × 40 mm

0.018 inch

6 Fr