Bur, Round, round shank 08227000

GUDID 24053613296131

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, reusable

• Primary Device ID: 24053613296131
• NIH Device Record Key: 8c196fe8-9f4d-40ec-aedb-53e86646f660
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bur, Round, round shank
• Version Model Number: 08227000
• Catalog Number: 08227000
• Company DUNS: 317409001
• Company Name: Gebr. Brasseler GmbH & Co. KG
• Device Count: 1
• DM Exempt: true
• 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: false
• 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	14053613296134 [Primary]
GS1	24053613296131 [Package]; Contains: 14053613296134; 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: 2026-03-19
• Device Publish Date: 2026-03-11

On-Brand Devices [Bur, Round, round shank]

• 24053613297220: 08228170
• 24053613296803: 08227750
• 24053613296131: 08227000
• 24053613295936: 08226790
• 24053613295929: 08226780