Dr. Sam Lee Ultimate Crestal&Lateral kit

GUDID 08800041054336

Surgident Co.,Ltd.

Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: 08800041054336
• NIH Device Record Key: efce2837-8796-4828-b504-3868311d4cf1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dr. Sam Lee Ultimate Crestal&Lateral kit
• Version Model Number: SD-SLU
• Company DUNS: 689846448
• Company Name: Surgident Co.,Ltd.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	08800041054336 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

[08800041054336]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-11
• Device Publish Date: 2023-10-03

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• 08800041065776 - Contra Torque: 2023-11-02