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Ns-3200

by Mercury Produzione Srl

Ref 2802Model NS-3200

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08052693520121 Basic UDI-DI 08052693520121UDI-DIDate21 Mar 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Nasofaringoscopio Endoflex Ns-3200
Model / Reference
NS-3200, 2802
Primary DI / UDI-DI
08052693520121
Basic UDI-DI
B-08052693520121
EMDN Code
Z12021006 Video nasopharyngo/laryngoscopes
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000030831

Other devices from Mercury Produzione Srl

  • Sf-17K1G

    Class IIa

  • Ns-4422

    Class IIa

  • Sf-10K2N

    Class IIa

  • Sf-30K2S

    Class IIa

  • Sf-17K2G

    Class IIa

  • Ns-3200U

    Class I

See all devices from Mercury Produzione Srl →

Properties

  • Reprocessed

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No