HEGAR Uterus Dilator double S-curved 15.0 mm / 16.0 mm

HEGAR UTERUS DILATOR • DOUBLE S-SHAPED • 15.0 MM / 16.0 MM • CE CLASS I • ISO 13485:2016

Extreme dilator for special maximum access procedures

The HEGAR Uterus Dilator double S-shaped 15.0 mm / 16.0 mm is a CE Class I medical device according to ISO 13485:2016. This extreme dilator enables ultimate cervical expansion for highly specialized operative gynecological procedures with maximum instrument diameter.

Product Highlights:

✔ Certified according to ISO 13485:2016
✔ CE Mark Class I (Directive 93/42/EEC)
✔ Extreme dilator 15.0 mm / 16.0 mm for maximum access
✔ Double S-shaped anatomy for optimal guidance
✔ High-quality stainless steel 1.4301 - rust-free and biocompatible
✔ Tested biocompatibility according to ISO 10993
✔ Ultra-attraumatic special tips
✔ Reinforced ergonomic safety ring handles
✔ Sterilizable and reusable

Advantages of the Extreme Dilator:

• Ultimate dilation: For highly specialized procedures with maximum instruments
• Optimal progression: Perfect gradation from 14.0 mm to 15.0 mm/16.0 mm
• Maximum stability: High-strength construction for extreme mechanical loads
• Precision guidance: Double S-curvature maintained even with extreme sizes
• Professional efficiency: Two extreme sizes in one instrument

Technical Specifications:

• Model: HEGAR Dilator double S-shaped
• Sizes: 15.0 mm / 16.0 mm (double-ended)
• Curvature: Double S-shaped, anatomically optimized
• Material: Surgical Steel 1.4301
• Tip form: Ultra-attraumatic, high-strength
• Handle design: Ergonomic with safety rings, maximum stability
• Risk Class: I according to Directive 93/42/EEC

Areas of Application:

• Ultimate cervical dilation for special maximum access
• Preparation for resectoscopes and large operative hysteroscopes
• Complex oncological procedures in gynecology
• Special surgical techniques with maximum instrumentation
• Extensive intrauterine surgical procedures

Important Safety Information:
• FOR HIGHLY SPECIALIZED GYNECOLOGICAL PROFESSIONALS ONLY
• Use only after complete gradual preliminary dilation up to 14.0 mm
• Extreme caution and slow, controlled dilation required
• Adequate anesthesia depth and muscle relaxation mandatory
• Continuous monitoring of tissue reaction
• Use only with absolutely compelling clinical indication
• Special reprocessing and sterilization controls required