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Trinity Acetabular Hip System 325.02.034

by Corin Ltd

Ref 325.02.034Model Trinity Dual Mobility ECiMa Inserts

Trinity Acetabular Hip System 325.02.034 is a constrained polyethylene acetabular liner (EU MDD Class IIb; FDA Class II) made by Corin Ltd, registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI B-05055343893517), cleared under FDA 510(k) K170359 on 31 Oct 2017 and listed in FDA GUDID since 16 Nov 2017 (UDI-DI 05055343893517), active as of 22 Oct 2026. One FDA recall is linked to it.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None ongoing

1 closed

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K170359

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05055343893517 Basic UDI-DI 05055343893517UDI-DIDate22 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05055343893517 UDI-DI Date16 Nov 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK170359 Date31 Oct 2017DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-05055343893517 registered 22 Sep 2026 Active
  • FDA 510(k) K170359 decided 31 Oct 2017 Active
  • FDA GUDID UDI-DI 05055343893517 listed 16 Nov 2017 Listed

Recalls

1 recall · FDA

    • Terminated Z-2608-2021 FDA Class II initiated 28 Jul 2021

    The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.

Timeline

4 dated events

  1. Cleared FDA 510(k) K170359
  2. Listed FDA GUDID 05055343893517
  3. Recall initiated FDA recalls Z-2608-2021
  4. Registered EUDAMED B-05055343893517

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Trinity Dual Mobility ECiMa insert size 2 EUDAMED
Trinity Acetabular Hip System GUDID
Generic name
Constrained polyethylene acetabular liner
Device name
Trinity Dual Mobility ECiMa inserts for use in Trinity Acetabular System
Model / Ref / Catalog
325.02.034, Trinity Dual Mobility ECiMa Inserts
Primary DI / UDI-DI
05055343893517
Basic UDI-DI
B-05055343893517
510(k) Number
FDA product code
LZO, MEH
EMDN code
P0908030502 Double-mobility acetabular components inserts
GMDN term
Constrained polyethylene acetabular liner
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3353
EU registration type
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 05055343893517: EUDAMED states No, FDA GUDID states Yes.

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: Constrained polyethylene acetabular liner

Cleared under the same submission (K170359)

and 8 more cleared under K170359

Similar devices in this category

Other devices filed under HIP PROSTHESES ACETABULAR COMPONENTS.

Other devices from Corin Ltd

See all devices from Corin Ltd →

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)