Maximum dilator with international scaling for special surgical procedures
The HANK Uterus Dilator double S-shaped 8.5 mm / 9.0 mm is a CE Class I medical device according to ISO 13485:2016. This maximum dilator with American scale (Fig. 17/18) enables maximum cervical dilation for special operative gynecological procedures with large-volume instruments.
Product Highlights:
✔ Certified according to ISO 13485:2016
✔ CE Mark Class I (Directive 93/42/EEC)
✔ Maximum dilator 8.5 mm / 9.0 mm with American scale
✔ International size designation: Fig. 17/18
✔ 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
✔ Ergonomic safety ring handles
✔ Sterilizable and reusable
Advantages of the Maximum Dilator:
• International compatibility: American scale for worldwide application
• Optimal size progression: Perfect gradation from 8.5 mm to 9.0 mm
• Maximum dilation: For special surgical procedures with large instruments
• Reinforced stability: Robust construction for high mechanical load capacity
• Clear identification: Internationally standardized size marking
Technical Specifications:
• Model: HANK Dilator double S-shaped
• Sizes: 8.5 mm / 9.0 mm (double-ended)
• American scale: Fig. 17/18
• Curvature: Double S-shaped, anatomically optimized
• Material: Surgical Steel 1.4301
• Tip form: Ultra-attraumatic
• Handle design: Ergonomic with safety rings
• Risk Class: I according to Directive 93/42/EEC
International Size Correspondence:
• 8.5 mm corresponds to American Scale Fig. 17
• 9.0 mm corresponds to American Scale Fig. 18
Areas of Application:
• Internationally standardized special surgical procedures
• Maximum cervical dilation for therapeutic curettages
• Preparation for large-caliber hysteroscopes
• Therapeutic dilation for strong cervical stenoses
• Surgical procedures with large-volume instruments
Important Safety Information:
• FOR EXPERIENCED GYNECOLOGICAL PROFESSIONALS ONLY
• Use only after complete gradual preliminary dilation
• Extreme care required during maximum expansion
• Ensure deep anesthesia
• Correctly interpret American scale designation
• Strictly follow reprocessing guidelines for reuse
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