Medium Radial Osteotome Blade 2500-10-754

GUDID 00847538009316

Medium Radial Osteotome Blade

SYMMETRY MEDICAL INC.

Orthopaedic osteotome

• Primary Device ID: 00847538009316
• NIH Device Record Key: d81ee6a1-413a-4350-8249-724b0738414c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medium Radial Osteotome Blade
• Version Model Number: 11-127-502
• Catalog Number: 2500-10-754
• Company DUNS: 079881212
• Company Name: SYMMETRY MEDICAL INC.
• 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	00847538009316 [Primary]

FDA Product Code

• GFI: Osteotome, Manual

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: 2023-10-02
• Device Publish Date: 2023-09-22

On-Brand Devices [Medium Radial Osteotome Blade]

• 00847538009309: Medium Radial Osteotome Blade
• 00847538009316: Medium Radial Osteotome Blade