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3M™ AlastiK™ 406-877

by 3M Unitek Corporation

Ref 406-877

3M™ AlastiK™ 406-877 is a device classified as Class IIa in the EU and Class I in the US made by 3M Unitek Corporation, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00652221076960) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00652221076960), active as of 7 Nov 2026.

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

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00652221076960 Basic UDI-DI 00652221076960UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00652221076960 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00652221076960 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 00652221076960 listed 8 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00652221076960
  2. Registered EUDAMED B-00652221076960

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
3M™ AlastiK™
Generic name
Orthodontic archwire/bracket ligature
Model / Ref / Catalog
406-877
Primary DI / UDI-DI
00652221076960
Basic UDI-DI
B-00652221076960
FDA product code
ECI
EMDN code
Q010406 Orthodontic ligatures
GMDN term
Orthodontic archwire/bracket ligature
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.5410
EU registration type
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 I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthodontic archwire/bracket ligature

Similar devices in this category

Other devices filed under ORTHODONTIC LIGATURES.

Other devices from 3M Unitek Corporation

See all devices from 3M Unitek Corporation →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)