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Acumed

by Acumed LLC 58 variants

Ref 80-4042

Acumed (80-4042) is a Class I device made by Acumed LLC, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-10806378117190), active as of 7 Nov 2026.

Active European Union

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-10806378117190 Basic UDI-DI 10806378117190UDI-DIDate29 Oct 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device name
Tray
Model / reference
80-4042
Primary DI / UDI-DI
10806378117190
Basic UDI-DI
B-10806378117190
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
US-MF-000023121
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Acumed LLC

See all devices from Acumed LLC →

Properties

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