SIMS Uterine Curette blunt and rigit Fig.0 6mm 31cm

SIMS UTERINE CURETTE BLUNT • FIG. 0 • 6MM • 31CM • CE CLASS I • ISO 13485:2016

Precision Uterine Curette for Tissue-Sparing Therapeutic Procedures

The SIMS Uterine Curette (Fig. 0, 6mm, 31cm) blunt and rigid is a medical device of CE Class I according to ISO 13485:2016. The instrument was developed for safe therapeutic procedures and offers optimal tissue protection while ensuring effective tissue removal.

Product Highlights:

✔ Certified according to ISO 13485:2016
✔ CE marking Class I (Directive 93/42/EEC)
✔ Optimal curette size 6mm (Fig. 0) – for standardized therapeutic procedures
✔ Ideal length 31cm – excellent accessibility of the uterine cavity
✔ High-quality stainless steel 1.4301 – rust-free and biocompatible
✔ Tested biocompatibility according to ISO 10993 – for maximum patient safety
✔ Blunt curette edge – for minimized perforation risk
✔ Rigid construction – for precise surgical work
✔ Robust manufacturing – for long-term reliable use
✔ Sterile packaged – individually for immediate use
✔ Reusable – when complying with reprocessing guidelines

Advantages of the SIMS Blunt Uterine Curette Fig. 0 31cm:

• Blunt design minimizes perforation risk
• Optimal size for safe standard therapeutic procedures
• Ideal length for good accessibility of the uterine cavity
• Rigid construction for precise and controlled work

Fields of Application:

• Therapeutic abrasion in patients with increased perforation risk
• Removal of residual tissue in abortus incompletus
• Tissue-sparing curettage in risk patients
• Therapeutic procedures in patients with thin endometrium

Technical Specifications:

• Model: SIMS Uterine Curette
• Type: Blunt and rigid, Figure 0
• Curette size: 6mm
• Length: 31cm
• Material: Surgical Steel 1.4301
• Design: Reusable
• Mechanism: Manual
• Risk Class: I according to Directive 93/42/EEC
• Sterilization: Sterile for single-use or reprocessable

Special Safety Notes:
• For trained gynecological medical personnel only
• Particularly suitable for patients with increased perforation risk
• Check for damage before use
• If reused, strict reprocessing guidelines must be observed