Shannon Recta Larga TM12220

GUDID 14053613291788

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use

• Primary Device ID: 14053613291788
• NIH Device Record Key: b1bf1633-cdf9-453e-a0e6-e464ba7da8e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shannon Recta Larga
• Version Model Number: TM12220
• Catalog Number: TM12220
• 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	14053613291788 [Primary]

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: 2024-08-06
• Device Publish Date: 2024-07-29

On-Brand Devices [Shannon Recta Larga]

• 14053613288405: DI222075R-S
• 24053613287917: P65-106-3030-S
• 14053613287675: MBUR2220
• 24053613288327: P65-105-2220-S
• 14053613291788: TM12220
• 14053613291399: TM13120
• 24053613290870: P65-106-3020-S