Specialty dilator for progressive cervical dilation
The GOODELL Uterus Dilator with a length of 34 cm is a CE Class I medical device according to ISO 13485:2016. This specialty dilator enables progressive, gentle cervical dilation through controlled pressure application for demanding gynecological procedures.
Product Highlights:
✔ Certified according to ISO 13485:2016
✔ CE Mark Class I (Directive 93/42/EEC)
✔ Specialty dilator with 34 cm length
✔ Progressive dilation technique through controlled pressure application
✔ High-quality stainless steel 1.4301 - rust-free and biocompatible
✔ Tested biocompatibility according to ISO 10993
✔ Atraumatic rounded tip
✔ Ergonomic grip elements
✔ Sterilizable and reusable
Advantages of the GOODELL Dilator:
• Progressive dilation: Gentle, controlled expansion through measured pressure application
• Optimal length: 34 cm for precise handling and sufficient reach
• Trauma reduction: Particularly gentle dilation technique compared to serial dilators
• Easy application: Direct, controlled pressure application without instrument changes
• Time efficiency: Rapid dilation in a continuous procedure
Technical Specifications:
• Model: GOODELL Uterus Dilator
• Length: 34 cm
• Diameter: Progressive increase according to Goodell principle
• Curvature: Anatomically adapted
• Material: Surgical Steel 1.4301
• Tip form: Atraumatic rounded
• Handle design: Ergonomic for precise pressure control
• Risk Class: I according to Directive 93/42/EEC
Special Features:
• Goodell principle: Progressive dilation through controlled pressure application
• Continuous process: No need to change between different dilators
• Tissue-sparing: Reduced trauma through even pressure distribution
Areas of Application:
• Progressive cervical dilation in obstetrics
• Therapeutic dilation for cervical stenoses
• Preparatory dilation before gynecological procedures
• Postpartum applications
• Special obstetric indications
Important Safety Information:
• FOR USE BY GYNECOLOGICAL PROFESSIONALS ONLY
• Use only for corresponding clinical indications
• Apply measured pressure under continuous control
• Check for damage before each use
• Ensure adequate lubrication
• Inform patient about the procedure
• Strictly follow reprocessing guidelines for reuse
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