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Clarity™ ADVANCED 006-260

by 3M Unitek Corporation

Ref 006-260

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

CE MDR CE MDD

Valid until

No date given

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number01979988401020000000059P3 Basic UDI-DI Date19 Jun 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number01979988401020000000059P3 Basic UDI-DI Date19 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00652221162199 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Clarity™ MBT™ EUDAMED
3M™ Clarity™ EUDAMED
Clarity™ ADVANCED GUDID
Generic name
Orthodontic bracket, ceramic
Device name
Clarity™ Advanced Ceramic Brackets
3M™ Clarity™ Advanced Ceramic Brackets, .018, LR5, -17T/2A, 006-260, 5/Pk
Model / Ref / Catalog
006-260
Primary DI / UDI-DI
00652221162199, 00197998365966
Basic UDI-DI
01979988401020000000059P3, B-00652221162199
Unit of use DI
00197998101984
FDA product code
NJM
EMDN code
Q010403 Orthodontic brackets and buttons
GMDN term
Orthodontic bracket, ceramic
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.5470
EU registration type
Standard device
Legacy device (under a directive)
EU 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 II

Related devices

Category: Orthodontic bracket, ceramic

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Properties

  • Single use
  • Prescription use
  • Lot / batch number

Other properties (22)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Reusable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No