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Pushbag Sacchetto di recupero laparoscopico

by MEDI-LINE S.r.l. EUDAMED

Active European Union

Ref 04-100Model Pushbag

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805511288K01020107MM Basic UDI-DIDate13 Apr 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CSQ0003220524 Supplemented

    Quality management system EU MDR

    Issued
    26 Nov 2024
    Expires
    27 Dec 2027
    Reason
    Add device or group

Specification

EUDAMED

Device Name
Pushbag Sacchetto di recupero laparoscopico
Model / Reference
Pushbag, 04-100
Primary DI / UDI-DI
08055112882022
Basic UDI-DI
805511288K01020107MM
EMDN Code
K01020107 Minimally invasive surgery recovery bags
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000019935

From the manufacturer

Manufacturer's product page: PUSHBAG

Other devices from MEDI-LINE S.r.l.

See all devices from MEDI-LINE S.r.l. →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No