Trinity Acetabular Hip System 321.100
by Corin Ltd
Ref 321.100Model Trinity Acetabular Shells
Trinity Acetabular Hip System 321.100 is a device classified as Class III in the EU and Class II in the US made by Corin Ltd, registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI B-05055343864609), cleared under FDA 510(k) K093472 on 23 Nov 2010 and listed in FDA GUDID since 17 Aug 2016 (UDI-DI 05055343864609), active as of 25 Oct 2026. One FDA recall is linked to it.
Active
Valid until
No date given
FDA recalls
None ongoingTrust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-05055343864609 05055343864609 | Date22 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05055343864609 | Date17 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK093472 | Date23 Nov 2010 | StatusActive |
Official records
- EUDAMED public site B-05055343864609
- AccessGUDID record 05055343864609
- FDA 510(k) database K093472
Across registries
- EUDAMED Basic UDI-DI B-05055343864609 registered 22 Sep 2026 Active
- FDA 510(k) K093472 decided 23 Nov 2010 Active
- FDA GUDID UDI-DI 05055343864609 listed 17 Aug 2016 Listed
Recalls
-
- Terminated Z-2604-2021
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
- Cleared FDA 510(k) K093472
- Listed FDA GUDID 05055343864609
- Recall initiated FDA recalls Z-2604-2021
- Registered EUDAMED B-05055343864609
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Trinity M10 Apical Hole Occluder EUDAMEDTrinity Acetabular Hip System GUDID
- Generic name
- Acetabulum prosthesis hole plug
- Device name
- Trinity Acetabular shells for use in Trinity Acetabular System
- Model / Ref / Catalog
- 321.100, Trinity Acetabular Shells
- Primary DI / UDI-DI
- 05055343864609
- Basic UDI-DI
- B-05055343864609
- 510(k) Number
- FDA product code
- LWJ, LZO, MEH
- EMDN code
- P090803010201 Primary implant uncemented metal acetabular cups
- GMDN term
- Acetabulum prosthesis hole plug
- Device class
- Class III EUDAMEDClass II GUDID
- Regulation number
- 888.3360, 888.3353
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Radiation Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class III | Class II |
| Sterilise before use | No | Yes |
Registry differences
EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:
- Sterilise before use UDI-DI 05055343864609: EUDAMED states No, FDA GUDID states Yes.
Device class is stated on each registry's own scale: Class III in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.
Similar devices in this category
Other devices filed under PRIMARY IMPLANT UNCEMENTED METAL ACETABULAR CUPS.
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- Acetabular Cup F13AB-PA00178 by WUHAN MINDRAY SCIENTIFIC CO., LTD.
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