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Multidirectional Threaded Peg 1312-11-111

by Biomet Orthopedics, Inc.

Ref 131211111

Multidirectional Threaded Peg 1312-11-111 (131211111) is a device classified as Class IIb in the EU and Class II in the US made by Biomet Orthopedics, Inc., registered in EUDAMED on 24 Oct 2026 (Basic UDI-DI B-00887868546556) and listed in FDA GUDID since 7 Sep 2022 (UDI-DI 00887868546556), 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-00887868546556 Basic UDI-DI 00887868546556UDI-DIDate24 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868546556 UDI-DI Date7 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00887868546556 registered 24 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868546556 listed 7 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868546556
  2. Registered EUDAMED B-00887868546556

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  • Withdrawn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
Multidirectional Threaded Peg
Generic name
Orthopaedic bone screw, non-bioabsorbable, non-sterile
Device name
Anatomic 2_5mm MD threaded peg
Model / Ref / Catalog
131211111, 1312-11-111
Primary DI / UDI-DI
00887868546556
Basic UDI-DI
B-00887868546556
FDA product code
KTT, LXT, HTY, HWC, HSB, HRS, HTN, JDW
EMDN code
P09120602 Cancellous screws
GMDN term
Orthopaedic bone screw, non-bioabsorbable, non-sterile
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3030, 888.3040, 888.3020
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
131211111
GUDID
1312-11-111
Device classEUDAMED
Class IIb
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

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

Related devices

Category: Orthopaedic bone screw, non-bioabsorbable, non-sterile

Similar devices in this category

Other devices filed under CANCELLOUS SCREWS.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
Other properties (20, all answered No)