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Reset Iq E.motion Pro

by Aesculap AG 11 variants

Part of a family of 44 devices: see the family page

Ref NP139R

Reset Iq E.motion Pro (NP139R) is a Class I device made by Aesculap AG, registered in EUDAMED on 25 Sep 2025 (Basic UDI-DI 4039239000000330ZL), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4039239000000330ZL Basic UDI-DI 04046964197246UDI-DIDate25 Sep 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
COLUMBUS instrument tray
Model / reference
NP139R
Primary DI / UDI-DI
04046964197246
Basic UDI-DI
4039239000000330ZL
Direct marketing DI
04046964197246
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Similar devices in this category

Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterilise before use
Other properties (13, all answered No)