Meniscus Versaflex 354-400

GUDID 07901125601062

GM DOS REIS INDUSTRIA E COMERCIO LTDA

Arthroscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 07901125601062
• NIH Device Record Key: 9eaf633d-b40b-41d7-a613-fc7bb142baad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Meniscus Versaflex
• Version Model Number: Meniscus Versaflex - Reverse
• Catalog Number: 354-400
• Company DUNS: 900865213
• Company Name: GM DOS REIS INDUSTRIA E COMERCIO LTDA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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	07901125601062 [Primary]

FDA Product Code

• GAT: Suture, Nonabsorbable, Synthetic, Polyethylene

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-11
• Device Publish Date: 2026-03-03

On-Brand Devices [Meniscus Versaflex]

• 07901125601062: Meniscus Versaflex - Reverse
• 07899258695846: Meniscus Versaflex