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3M™ V.a.c.®

by KCI USA Inc.

Ref ULTDEV01/EUV011

3M™ V.a.c.® (ULTDEV01/EUV011) is a Class IIa device made by Kci USA, Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 0849554084010100000003166), active as of 7 Nov 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 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/MDR Number0849554084010100000003166 Basic UDI-DI 50849554016175UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 0849554084010100000003166 — open Devices and search for it

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
3M™ V.A.C.® Ulta Therapy Unit
Model / reference
ULTDEV01/EUV011
Primary DI / UDI-DI
50849554016175
Basic UDI-DI
0849554084010100000003166
EMDN code
Z12040205 Vacuum medication equipment
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000016844
Authorised representative
KCI Manufacturing Unlimited Company IE-AR-000016082

Similar devices in this category

Other devices filed under GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS.

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Properties

  • Administering medicine
  • Measuring function
Other properties (12, all answered No)