Skip to content

REVISION Hip Lateralized Trial Neck with Screw

by Limacorporate 7 variants

Ref 9038.10.760Model 80333902A014BK, REVISION Hip - Lateralized Trial Neck H60 with Screw

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

CE MDR CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 7 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number80333902A014BK Basic UDI-DI 08033390112895UDI-DIDate29 Oct 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number80333902A014BK Basic UDI-DI 08033390112895UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08033390112895 UDI-DI Date12 Apr 2016ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 7 Nov 2026.

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  • Withdrawn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
REVISION Hip - Lateralized Trial Neck H60 with Screw EUDAMED
REVISION Hip GUDID
Generic Name
Femoral stem prosthesis trial
Model / Ref / Catalog
80333902A014BK, 9038.10.760, REVISION Hip - Lateralized Trial Neck H60 with Screw, Lateralized Trial Neck with Screw
Primary DI / UDI-DI
08033390112895
Basic UDI-DI
80333902A014BK, B-08033390112895
510(k) Number
FDA Product Code
LZO, KWY, LPH
EMDN Code
V06010101 Hip prostheses testing devices
GMDN Term
Femoral stem prosthesis trial
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
888.3353, 888.3390, 888.3358
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
80333902A014BK
9038.10.760
REVISION Hip - Lateralized Trial Neck H60 with Screw
GUDID
Lateralized Trial Neck with Screw
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Femoral stem prosthesis trial

Cleared under the same submission (K151739)

Show all (12)

Other devices from Limacorporate

See all devices from Limacorporate →

Properties

  • Reusable
  • Prescription Use
  • Lot / Batch Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No