NASAL/TENDON KNIFE 1271-152

GUDID 00192896057159

NASAL/TENDON KNIFE DOUBLE LANCE STRAIGHT EDGE

SONTEC INSTRUMENTS, INC.

Orthopaedic osteotome blade, reusable

• Primary Device ID: 00192896057159
• NIH Device Record Key: 4601910a-12f4-4b89-a4a6-369fe698f1b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NASAL/TENDON KNIFE
• Version Model Number: 1271-152
• Catalog Number: 1271-152
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 6.5 Inch
• Length: 6.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896057159 [Primary]

FDA Product Code

• HTS: Knife, Orthopedic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896057159]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-11-08
• Device Publish Date: 2018-10-08

On-Brand Devices [NASAL/TENDON KNIFE]

• 00192896057272: NASAL/TENDON KNIFE SINGLE RETROGRAD CURVED EDGE
• 00192896057265: NASAL/TENDON KNIFE SINGLE LANCE STRAIGHT EDGE
• 00192896057241: NASAL/TENDON KNIFE SINGLE CLASSIC STRAIGHT EDGE
• 00192896057234: NASAL/TENDON KNIFE SINGLE STRAIGHT EDGE
• 00192896057159: NASAL/TENDON KNIFE DOUBLE LANCE STRAIGHT EDGE
• 00192896115347: Nasal/Tendon Knife Double Lance Edge Straight Blade Ceramic Coating