C2 REVISION Hip 9045.10.280

GUDID 08033390024938

M8 Stem Beater-Extractor

LIMACORPORATE SPA

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 08033390024938
• NIH Device Record Key: 8de24e81-a02e-4ca7-9009-ea2ce92f5bc2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: C2 REVISION Hip
• Version Model Number: 9045.10.280
• Catalog Number: 9045.10.280
• 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	08033390024938 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170473

FDA Product Code

• LWJ: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

Sterilization

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

[08033390024938]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-04-23
• Device Publish Date: 2018-03-13

On-Brand Devices [C2 REVISION Hip]

• 08033390024938: M8 Stem Beater-Extractor
• 08033390024891: Straight Handle for Rasp