MODULUS Femoral Stem 9043.10.310

GUDID 08033390024730

Manual impactor

LIMACORPORATE SPA

Orthopaedic implant impactor, reusable

• Primary Device ID: 08033390024730
• NIH Device Record Key: f46a61cd-1050-40f8-bf79-36ab9c61c33c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MODULUS Femoral Stem
• Version Model Number: 9043.10.310
• Catalog Number: 9043.10.310
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390024730 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[08033390024730]

Moist Heat or Steam Sterilization

[08033390024730]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2026-02-09
• Device Publish Date: 2018-09-21

On-Brand Devices [MODULUS Femoral Stem]

• 08033390085915: Stem Impactor
• 08033390024730: Manual impactor