Shannon Recta X-Larga G01 S5330

GUDID 24053613295721

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use

• Primary Device ID: 24053613295721
• NIH Device Record Key: cc4626d1-a12a-4971-ba4d-3a50a3cabf35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shannon Recta X-Larga
• Version Model Number: G01 S5330
• Catalog Number: G01 S5330
• 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	14053613295724 [Primary]
GS1	24053613295721 [Package]; Contains: 14053613295724; 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: 2026-02-02
• Device Publish Date: 2026-01-23

On-Brand Devices [Shannon Recta X-Larga]

• 24053613288440: DS3030100R-S
• 24053613288341: P65-105-3030-S
• 14053613292679: MBUR3030
• 24053613293390: P65-105-3031-S
• 24053613295721: G01 S5330