Brophy, round shank MBUR5015

GUDID 14053613292921

Brophy 5.0 x 15.2 x 70 mm, Foot cutter

Gebr. Brasseler GmbH & Co. KG

Orthopaedic bur, single-use

• Primary Device ID: 14053613292921
• NIH Device Record Key: e8f3dd74-3c44-416b-9402-6f3ba23c6c1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Brophy, round shank
• Version Model Number: MBUR5015
• Catalog Number: MBUR5015
• 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	14053613292921 [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: 2025-07-25
• Device Publish Date: 2025-07-17

On-Brand Devices [Brophy, round shank]

• 14053613292921: Brophy 5.0 x 15.2 x 70 mm, Foot cutter
• 24053613290979: AR-301-B103