Neck Extractor 9042.15.240

GUDID 08033390114790

Neck Extractor - H-MAX S Instrument

LIMACORPORATE SPA

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 08033390114790
• NIH Device Record Key: 2fa012f0-9699-424d-90d2-75524d59ba6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neck Extractor
• Version Model Number: Neck Extractor
• Catalog Number: 9042.15.240
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	08033390114790 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112091

FDA Product Code

• MEH: Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate

Sterilization

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

[08033390114790]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-04-23
• Device Publish Date: 2016-07-27

On-Brand Devices [Neck Extractor]

• 08033390114790: Neck Extractor - H-MAX S Instrument
• 08033390085274: Neck Extractor