Reprocessed Sagittal Saw Blade, 90 x 19 x 1.27mm

GUDID B390S8966561

SURETEK MEDICAL

Surgical saw blade, sagittal, reprocessed

• Primary Device ID: B390S8966561
• NIH Device Record Key: a06bc76f-440f-4d7c-9836-3b11d7aab96f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed Sagittal Saw Blade, 90 x 19 x 1.27mm
• Version Model Number: S89-6656
• 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	B390S8966561 [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: 2024-12-23
• Device Publish Date: 2024-12-13

On-Brand Devices [Reprocessed Sagittal Saw Blade, 90 x 19 x 1.27mm]

• B390S8936561: S89-3656
• B390S8966561: S89-6656