Directa Cheek Retractor 511582

GUDID 17310235115821

Directa AB

Hand-held dental retractor

• Primary Device ID: 17310235115821
• NIH Device Record Key: 538e85fd-1fb8-4fcb-b240-2f57741a87a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Directa Cheek Retractor
• Version Model Number: Translucent Adult
• Catalog Number: 511582
• Company DUNS: 353954381
• Company Name: Directa AB
• 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: true
• 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	17310235115821 [Primary]

FDA Product Code

• EGZ: Holder, Film, X-Ray

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-13
• Device Publish Date: 2022-12-05

On-Brand Devices [Directa Cheek Retractor ]

• 17310235115821: Translucent Adult
• 17310235115913: Ivory Child
• 17310235115906: Ivory Adult
• 17310235115890: Clear Child
• 17310235115883: Clear Adult
• 17310235115876: Red Child
• 17310235115869: Red Adult
• 17310235115852: Blue Child
• 17310235115845: Blue Adult
• 17310235115838: Translucent Child