Wedge 3 DW311065R-S

GUDID 24053613288419

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use

• Primary Device ID: 24053613288419
• NIH Device Record Key: cf9f51c6-4cd3-46a3-86e1-a6de74fe4d4a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Wedge 3
• Version Model Number: DW311065R-S
• Catalog Number: DW311065R-S
• Company DUNS: 317409001
• Company Name: Gebr. Brasseler GmbH & Co. KG
• 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: 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	14053613288412 [Primary]
GS1	24053613288419 [Package]; Contains: 14053613288412; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• GFF: Bur, Surgical, General & Plastic Surgery

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: 2024-03-07
• Device Publish Date: 2024-02-28

On-Brand Devices [Wedge 3]

• 24053613288419: DW311065R-S
• 14053613287484: MBUR2913
• 24053613288365: P65-108-2913-S
• 14053613291214: TM22913
• 14053613291207: TM12913