Shannon Recta P65-106-2220-S

GUDID 24053613287887

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use

• Primary Device ID: 24053613287887
• NIH Device Record Key: 33a375cb-6253-4627-8256-001fb2d02ab5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shannon Recta
• Version Model Number: P65-106-2220-S
• Catalog Number: P65-106-2220-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	14053613287880 [Primary]
GS1	24053613287887 [Package]; Contains: 14053613287880; 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: 2024-04-03
• Device Publish Date: 2024-03-26

On-Brand Devices [Shannon Recta]

• 24053613287887: P65-106-2220-S
• 24053613287863: P65-106-2020-S
• 14053613287453: MBUR2013
• 24053613288334: P65-105-2013-S
• 14053613291795: TM12013