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Adaptor Delta Cups

by Limacorporate 3 variants

Part of a family of 85 devices: see the family page

Ref 9055.51.053Model 80333902A059C9, DELTA Cup - Adapter for Curved Impactor # LARGE

Adaptor Delta Cups (9055.51.053) is a device classified as Class IIa and Class I in the EU and Class II in the US made by Limacorporate, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 80333902A059C9) and listed in FDA GUDID since 17 Jun 2016 (UDI-DI 08033390104852), active as of 7 Nov 2026.

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

CE MDR 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 Number80333902A059C9 Basic UDI-DI 08033390104852UDI-DIDate29 Oct 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number80333902A059C9 Basic UDI-DI 08033390104852UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08033390104852 UDI-DI Date17 Jun 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 80333902A059C9 registered 29 Oct 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 08033390104852 listed 17 Jun 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08033390104852
  2. Registered EUDAMED 80333902A059C9

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
DELTA Cup - Adapter for Curved Impactor # LARGE EUDAMED
Adaptor Delta Cups GUDID
Generic name
Orthopaedic implant-instrument extension adaptor, reusable
Model / Ref / Catalog
80333902A059C9, 9055.51.053, DELTA Cup - Adapter for Curved Impactor # LARGE, Adaptor
Primary DI / UDI-DI
08033390104852
Basic UDI-DI
80333902A059C9, B-08033390104852
FDA product code
LPH, MBL
EMDN code
L091104, L091199
GMDN term
Orthopaedic implant-instrument extension adaptor, reusable
Device class
Class IIa EUDAMED
Class I EUDAMED
Class II GUDID
Regulation number
888.3358
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
80333902A059C9
9055.51.053
DELTA Cup - Adapter for Curved Impactor # LARGE
GUDID
Adaptor
Device classEUDAMED
Class IIa
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa and Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes.

Related devices

Category: Orthopaedic implant-instrument extension adaptor, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE.

Other devices from Limacorporate

See all devices from Limacorporate →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)