ENDOLARYNGEAL KNIFE 1301-506

GUDID 00192896058682

ENDOLARYNGEAL KNIFE MICROSCOPIC OVAL ROUND EDGE BLADE

SONTEC INSTRUMENTS, INC.

Laryngeal knife

• Primary Device ID: 00192896058682
• NIH Device Record Key: 2d9b4b4f-2714-4191-a0a9-e81f27e78317
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDOLARYNGEAL KNIFE
• Version Model Number: 1301-506
• Catalog Number: 1301-506
• 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: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 10 Inch
• Length: 10 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896058682 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[00192896058682]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-11-22
• Device Publish Date: 2018-09-27

On-Brand Devices [ENDOLARYNGEAL KNIFE]

• 00192896058705: ENDOLARYNGEAL PROBE MICROSCOPIC STRAIGHT BUTTON-END
• 00192896058682: ENDOLARYNGEAL KNIFE MICROSCOPIC OVAL ROUND EDGE BLADE