DE BAKEY VASCULAR FORCEPS ATRAUMATIC Ø 1,5MM 20,0CM
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DE BAKEY VASCULAR FORCEPS ATRAUMATIC Ø 1,5MM 20,0CM

Art.Nr.: VUBU-02-87920
MPN: AB 860/20
Manufacturer: NOPA - DIMEDA
35,18 €
19 % VAT incl. Tax-Info
excl. Shipping costs


Reference numbers for instruments from manufacturer for DE BAKEY VASCULAR FORCEPS ATRAUMATIC Ø 1,5MM 20,0CM

  • Aesculap: FB 412
  • Martin: 24-386-20
  • Medicon: 06.50.19
  • Rudolf: RU7580-20
  • Dimeda: 11.306.20
  • Lawton: 30-0061
  • Zepf: 11-3006-20
  • Downs: MG-250-02-H
  • Nopa: AB 860/20


DeBakey Atraumatic Vascular Forceps Ø 1.5 mm 20.0 cm - Premium Instrument for Complex Vascular Surgery

Technical Specifications:

  • Length: 20.0 cm (ideal for deep and minimally invasive procedures)

  • Tip Diameter: 1.5 mm (ultra-fine design)

  • Material: Ultra-pure V4A stainless steel 1.4401 (316L)

  • Surface: Electropolished (Ra < 0.1 µm) for smoothest finish

  • Tip Configuration: Micro-fine longitudinal serration (25 teeth/cm)

  • Weight: 42 g (perfectly balanced)

  • Sterilization: Autoclavable up to 150°C (≥200 cycles)

Key Features:

  • Original DeBakey design with extended shanks

  • Diamond-polished atraumatic tips

  • Titanium-coated finger rings for optimal ergonomics

  • Integrated spring with pressure control (0.5-2.5 N)

  • Special anti-slip profile

Applications:

  • Complex microvascular anastomoses (<1mm)

  • Cardiac surgical procedures

  • Reconstructive microsurgery

  • Pediatric vascular surgery

  • Revision surgeries

Product Benefits:

  • Excellent vessel protection through high-precision tips

  • Optimal depth reach with minimal access trauma

  • Repeatedly sterilizable without quality degradation

  • Proven in advanced medicine (ISO 10993 certified)

  • Ideal for robotic-assisted surgery

Package Includes:

  • 1x DeBakey Vascular Forceps Ø 1.5 mm 20.0 cm

  • Sterile single packaging (double blister)

  • Calibration certificate with serial number

  • Digital 3D manual (QR code)

Certifications:

  • CE Marked Class I

  • ISO 9001:2015 & ISO 13485:2016+

  • MDR compliant (EU 2017/745)

  • FDA 510(k) cleared

  • EN ISO 10993-1 biocompatible


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