GUIDE PIN & GUIDE SCREW SET OC06D.067.032 STE

GUDID 24053613284374

Gebr. Brasseler GmbH & Co. KG

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• Primary Device ID: 24053613284374
• NIH Device Record Key: 7b5e3b13-a979-40c0-8c79-8fbbcebc6d4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUIDE PIN & GUIDE SCREW SET
• Version Model Number: OC06D.067.032
• Catalog Number: OC06D.067.032 STE
• Company DUNS: 317409001
• Company Name: Gebr. Brasseler GmbH & Co. KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	14053613284377 [Primary]
GS1	24053613284374 [Package]; Contains: 14053613284377; Package: [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131264

FDA Product Code

• HWC: Screw, Fixation, Bone

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: 2021-03-09
• Device Publish Date: 2021-03-01

On-Brand Devices [GUIDE PIN & GUIDE SCREW SET]

• 24053613284374: OC06D.067.032
• 24053613285548: OC06D.076.032
• 24053613287221: GS06D.067.032