Wedge 3 Round shank P65-106-2913-S

GUDID 24053613287801

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use

• Primary Device ID: 24053613287801
• NIH Device Record Key: 0e9daf76-bbcf-4e51-a895-30b89f01d77d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Wedge 3 Round shank
• Version Model Number: P65-106-2913-S
• Catalog Number: P65-106-2913-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	14053613287804 [Primary]
GS1	24053613287801 [Package]; Contains: 14053613287804; Package: [1 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: 2024-02-12
• Device Publish Date: 2024-02-02

On-Brand Devices [Wedge 3 Round shank]

• 24053613287801: P65-106-2913-S
• 14053613289563: M31652