Logical Lateralised Liner – 10° Hood Vit-E

GUDID 09348215133320

SIGNATURE ORTHOPAEDICS PTY LTD

Non-constrained polyethylene acetabular liner

• Primary Device ID: 09348215133320
• NIH Device Record Key: 55835689-a1f9-4de9-ab49-02fc514ca7ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Logical Lateralised Liner – 10° Hood Vit-E
• Version Model Number: 111-12-8660E
• Company DUNS: 751993028
• Company Name: SIGNATURE ORTHOPAEDICS PTY LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	09348215133320 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121297

FDA Product Code

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

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-11
• Device Publish Date: 2024-10-03

On-Brand Devices [Logical Lateralised Liner – 10° Hood Vit-E ]

• 09348215133344: 111-12-8460E
• 09348215133337: 111-12-8456E
• 09348215133320: 111-12-8660E
• 09348215133313: 111-12-8656E
• 09348215133306: 111-12-8652E
• 09348215133290: 111-12-8260E
• 09348215133283: 111-12-8256E
• 09348215133276: 111-12-8252E
• 09348215133269: 111-12-8250E
• 09348215133252: 111-12-8852E
• 09348215133245: 111-12-8850E
• 09348215133238: 111-12-8844E
• 09348215133221: 111-12-8240E