Skip to content

JuggerLoc™ 110027357

by Biomet Orthopedics, Inc.

Ref 110027357

JuggerLoc™ 110027357 is a device classified as Class IIa in the EU and Class I in the US made by Biomet Orthopedics, Inc., registered in EUDAMED on 19 Oct 2026 (Basic UDI-DI B-00880304857254) and listed in FDA GUDID since 2 Mar 2018 (UDI-DI 00880304857254), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00880304857254 Basic UDI-DI 00880304857254UDI-DIDate19 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00880304857254 UDI-DI Date2 Mar 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00880304857254 registered 19 Oct 2026 Active
  • FDA GUDID UDI-DI 00880304857254 listed 2 Mar 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00880304857254
  2. Registered EUDAMED B-00880304857254

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  • Withdrawn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
JuggerLoc™
Generic name
General surgical procedure kit, non-medicated, single-use
Device name
JLoc 2_9 Disposable Cannula Kit
Model / Ref / Catalog
110027357
Primary DI / UDI-DI
00880304857254
Basic UDI-DI
B-00880304857254
FDA product code
KDD
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
General surgical procedure kit, non-medicated, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4800
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
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: General surgical procedure kit, non-medicated, single-use

Similar devices in this category

Other devices filed under ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

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