Modulus Hip System 9043.10.350

GUDID 08033390030809

Neck Impactor

LIMACORPORATE SPA

Orthopaedic implant impactor, reusable
Primary Device ID08033390030809
NIH Device Record Key86268629-6bdf-4177-874a-19c88d68dbb6
Commercial Distribution StatusIn Commercial Distribution
Brand NameModulus Hip System
Version Model NumberNeck Impactor
Catalog Number9043.10.350
Company DUNS432066322
Company NameLIMACORPORATE SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108033390030809 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWZProsthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


[08033390030809]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2026-02-09
Device Publish Date2016-04-15

On-Brand Devices [Modulus Hip System]

08033390030816Neck Extractor
08033390030809Neck Impactor

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