DIRECTION INDICATOR Ø4.3XØ2.0MM SHORT

GUDID 07899995265234

DIRECTION INDICATOR Ø4.3XØ2.0MM SHORT

Sin Sistema de Implante Nacional S/A

Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable Dental implantation depth/angle gauge, reusable

• Primary Device ID: 07899995265234
• NIH Device Record Key: 7f1c9597-8ef2-49c1-862a-5b8cad9ce01b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIRECTION INDICATOR Ø4.3XØ2.0MM SHORT
• Version Model Number: ID 4320C
• Company DUNS: 904569092
• Company Name: Sin Sistema de Implante Nacional S/A
• 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: true
• 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	07899995265234 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

[07899995265234]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-01
• Device Publish Date: 2023-12-22

Devices Manufactured by Sin Sistema de Implante Nacional S/A

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• 07899995201270 - DRIVER HANDPIECE IMP. TRYON GUIDED: 2024-01-01 DRIVER HANDPIECE IMP. TRYON GUIDED
• 07899995203120 - DRIVE ANGLED BONE GRAFT: 2024-01-01 DRIVE ANGLED BONE GRAFT
• 07899995203144 - DRIVER ORTHODONTIC: 2024-01-01 DRIVER ORTHODONTIC
• 07899995205049 - CHAVE DE CATRACA: 2024-01-01 CHAVE DE CATRACA
• 07899995206282 - DRIVER HANDPIECE IMP. CM: 2024-01-01 DRIVER HANDPIECE IMP. CM
• 07899995206299 - DRIVER HANDPIECE IMP. CM: 2024-01-01 DRIVER HANDPIECE IMP. CM
• 07899995207203 - DRIVER HANDPIECE IMP. 24MM: 2024-01-01 DRIVER HANDPIECE IMP. 24MM