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Acumed

by Acumed LLC 64 variants

Ref 7107-0602

Acumed (7107-0602) is a Class IIa device made by Acumed LLC, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-10806378105104), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-10806378105104 Basic UDI-DI 10806378105104UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Trial
Model / reference
7107-0602
Primary DI / UDI-DI
10806378105104
Basic UDI-DI
B-10806378105104
EMDN code
L091099 Osteosynthesis instruments, reusable - other
Device class
Class IIa
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
  • Reusable
Other properties (12, all answered No)