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JuggerStitch® 110031679

by Biomet Orthopedics, Inc.

Ref 110031679

JuggerStitch® 110031679 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 889024APA24) and listed in FDA GUDID since 17 Sep 2019 (UDI-DI 00887868245022), active as of 23 Oct 2026.

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

CE MDR

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number889024APA24 Basic UDI-DI 00887868245022UDI-DIDate19 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868245022 UDI-DI Date17 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 889024APA24 registered 19 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868245022 listed 17 Sep 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868245022
  2. Registered EUDAMED 889024APA24

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
JuggerStitch®
Generic name
Suture trimmer
Device name
JuggerStitch Suture Cutter
Model / Ref / Catalog
110031679
Primary DI / UDI-DI
00887868245022
Basic UDI-DI
889024APA24
FDA product code
NBH
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
GMDN term
Suture trimmer
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.1100
EU registration type
Standard device
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: Suture trimmer

Similar devices

Also classified as Suture trimmer.

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)