Reprocessed Sagittal Saw Blade, 90 x 25 x 1.27mm

GUDID B3906125127901

SURETEK MEDICAL

Surgical power tool system handpiece, sawing, line-powered

• Primary Device ID: B3906125127901
• NIH Device Record Key: 57f0e81e-7613-4034-8839-6b986e563d8e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed Sagittal Saw Blade, 90 x 25 x 1.27mm
• Version Model Number: 6125-127-90
• Company DUNS: 785616934
• Company Name: SURETEK MEDICAL
• 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: false
• 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
HIBCC	B3906125127901 [Primary]

FDA Product Code

• GFA: Blade, Saw, General & Plastic Surgery, Surgical

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: 2021-05-28
• Device Publish Date: 2021-05-20

On-Brand Devices [Reprocessed Sagittal Saw Blade, 90 x 25 x 1.27mm]

• B3906125127901: 6125-127-90
• B39061251271001: 6125-127-100