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Sub

by EMED Technologies Corporation

Ref SUB-612-G24

Sub (SUB-612-G24) is a Class IIa device made by EMED Technologies Corporation, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-00817708021875), 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-00817708021875 Basic UDI-DI 00817708021875UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
SUB-612-G24
Primary DI / UDI-DI
00817708021875
Basic UDI-DI
B-00817708021875
EMDN code
Z12030385 Infusion instruments - consumables
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000012148
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

Other devices filed under INFUSION INSTRUMENTS - CONSUMABLES.

Other devices from EMED Technologies Corporation

See all devices from EMED Technologies Corporation →

Properties

  • Supplied sterile
  • Administering medicine
Other properties (12, all answered No)