Ceramic Liner Inserter Impactor Head

GUDID 09348215039356

SIGNATURE ORTHOPAEDICS PTY LTD

Orthopaedic implant impactor, reusable

• Primary Device ID: 09348215039356
• NIH Device Record Key: 9909cc86-9471-4c8c-b149-69f1dd110f90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ceramic Liner Inserter Impactor Head
• Version Model Number: 112-152-212
• Company DUNS: 751993028
• Company Name: SIGNATURE ORTHOPAEDICS PTY LTD
• 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	09348215039356 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[09348215039356]

Moist Heat or Steam Sterilization

[09348215039356]

Moist Heat or Steam Sterilization

[09348215039356]

Moist Heat or Steam Sterilization

[09348215039356]

Moist Heat or Steam Sterilization

[09348215039356]

Moist Heat or Steam Sterilization

[09348215039356]

Moist Heat or Steam Sterilization

[09348215039356]

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: 2018-10-09

On-Brand Devices [Ceramic Liner Inserter Impactor Head]

• 09348215039363: 112-152-213
• 09348215039356: 112-152-212
• 09348215039349: 112-152-211
• 09348215039332: 112-152-210