Starter

GUDID 07640181161522

Keri Medical 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

• Primary Device ID: 07640181161522
• NIH Device Record Key: f2232e42-2418-4a54-bcff-cf914a525182
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Starter
• Version Model Number: 211-A30000
• Company DUNS: 480138827
• Company Name: Keri Medical 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640181161522 [Primary]

FDA Product Code

• HWD: Starter, Bone Screw

Sterilization

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

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

[07640181161522]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-30
• Device Publish Date: 2022-11-22

Devices Manufactured by Keri Medical SA

• 07640181161409 - Pattern MCP 00: 2022-11-30
• 07640181161416 - Pattern MCP 10: 2022-11-30
• 07640181161423 - Pattern MCP 20: 2022-11-30
• 07640181161430 - Pattern MCP 30: 2022-11-30
• 07640181161447 - Pattern MCP 40: 2022-11-30
• 07640181161454 - Pattern MCP 50: 2022-11-30
• 07640181161461 - Pattern MCP 60: 2022-11-30
• 07640181161478 - Pattern PIP 1: 2022-11-30