Surgical Manual Instrument

GUDID 07630542731044

Tibia stylus 2/8 with button

Medacta International SA

Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 07630542731044
• NIH Device Record Key: 8ba42ef3-4562-4dfb-ad2c-fa6485ff0452
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgical Manual Instrument
• Version Model Number: 02.12.10.2951
• Company DUNS: 488227125
• Company Name: Medacta International SA
• 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	07630542731044 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

[07630542731044]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-22
• Device Publish Date: 2024-04-12

On-Brand Devices [Surgical Manual Instrument ]

• 07630971254466: Femoral Impactor/Extractor S4-7
• 07630345785626: Tap for Glenoid Polyaxial screw
• 07630542721373: MUST LT distractor frame
• 07630542731044: Tibia stylus 2/8 with button