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EndoScan

by Deka M.E.L.A. SRL

Part of a family of 41 devices: see the family page

Ref F26801

EndoScan (F26801), a medical device (EU MDR Class IIb; EMDN category laser surgery instruments) made by Deka M.E.L.A. SRL, was registered in EUDAMED on 16 Dec 2021 (Basic UDI-DI 803410851F49801KD); the registry lists it as withdrawn as of 23 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803410851F49801KD Basic UDI-DI 08034108511429UDI-DIDate16 Dec 2021RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device name
Scanning units for CO2 lasers
Model / reference
F26801
Primary DI / UDI-DI
08034108511429
Basic UDI-DI
803410851F49801KD
EMDN code
Z12011099 Laser surgery instruments - other
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007389

Similar devices in this category

Other devices filed under LASER SURGERY INSTRUMENTS - OTHER.

Other devices from Deka M.E.L.A. SRL

See all devices from Deka M.E.L.A. SRL →

Properties

Other properties (14, all answered No)