Skip to content

3M™ Unitek™ Victory Series™ 067-911

by 3M Unitek Corporation

Ref 067-911

Active European Union. Also listed in GUDID (US).

CE MDR CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number01979988401020000000076P3 Basic UDI-DI Date3 Sep 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number01979988401020000000076P3 Basic UDI-DI Date3 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00652221022035 UDI-DI Date18 Oct 2018ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Solventum™ Victory Series™ EUDAMED
3M™ Victory Series™ EUDAMED
3M™ Unitek™ Victory Series™ GUDID
Generic Name
Orthodontic tube
Device Name
Victory Series™ Buccal Tubes | Victory Series™ Superior Fit Buccal Tubes
3M™ Victory Series™ Buccal Tubes, .022, LL6, Convertible Triple, -25T/5Off, 067-911, Ea
Model / Ref / Catalog
067-911
Primary DI / UDI-DI
00652221022035, 00197998259937
Basic UDI-DI
01979988401020000000076P3, B-00652221022035
FDA Product Code
DZD
EMDN Code
Q010403 Orthodontic brackets and buttons
GMDN Term
Orthodontic tube
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
872.5410
Market of Registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I

Related devices

Category: Orthodontic tube

Other devices from 3M Unitek Corporation

See all devices from 3M Unitek Corporation →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (20)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No