Various external fixator kits and accessories AI

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Subject of procurement

  • Object: Various external fixator kits and accessories.
  • Technical requirements:
    • Products must comply with the European Medical Device Regulation (MDR) 2017/745 and bear the CE mark.
    • Unique Device Identification (UDI) is required.
    • Implants must be complete, made of titanium or stainless steel (connecting rods may also be carbon).
    • Instrumentation must be disinfectable and sterilizable.
  • Location: Tallinn, Estonia (EE001).

Contract terms

  • Duration: 48 months…
     
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314675_ESPD_v2.0_laiendatud.xml

314675_hankepass_taiendavate_selgitustega.pdf

314675_hindamiskriteeriumid.pdf

314675_vastavustingimused.pdf

314675.zip

Lisa 1_Tehniline kirjeldus.docx

Lisa 2_Maksumuse vorm.xlsx

Lisa 3_Lepingu projekt.docx

RHAD üldosa.docx

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