FenderWedge 602735

GUDID 17310236027352

Directa AB

Dental wedge, single-use

• Primary Device ID: 17310236027352
• NIH Device Record Key: 446a7f94-bcb7-4b89-86cf-003fbc0fb415
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FenderWedge
• Version Model Number: NG Purple
• Catalog Number: 602735
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	17310236027352 [Primary]

FDA Product Code

• EJB: Handle, Instrument, Dental

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: 2022-12-14
• Device Publish Date: 2022-12-06

On-Brand Devices [FenderWedge ]

• 17310236027369: NG Orange
• 17310236027352: NG Purple
• 17310236028113: Prep Value Pack
• 17310236028038: Value Pack
• 17310236028021: Value Pack
• 17310236028014: Value Pack
• 17310236028007: Value Pack
• 17310236027543: X-small
• 17310236027536: Large
• 17310236027529: Medium
• 17310236027512: Small
• 17310236027505: Assortment
• 17310236027499: Prep