SONTEC EAR RASPATORY 475-596

GUDID 00192896042513

SONTEC EAR RASPATORY SERRATED CURVED LEFT SHAFT

SONTEC INSTRUMENTS, INC.

Middle ear file/rasp

• Primary Device ID: 00192896042513
• NIH Device Record Key: 2f64ee18-9879-4a4e-9422-cdd08226152f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONTEC EAR RASPATORY
• Version Model Number: 475-596
• Catalog Number: 475-596
• 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: 6 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896042513 [Primary]

FDA Product Code

• JYY: RASP, EAR

Sterilization

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

[00192896042513]

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: 2018-12-07
• Device Publish Date: 2018-09-14

On-Brand Devices [SONTEC EAR RASPATORY]

• 00192896080157: SONTEC EAR RASPATORY RIGHT CURVED TIP
• 00192896042544: SONTEC EAR RASPATORY SERRATED CURVED RIGHT SHAFT
• 00192896042537: SONTEC EAR RASPATORY SERRATED CURVED LEFT SHAFT
• 00192896042520: SONTEC EAR RASPATORY SERRATED CURVED RIGHT SHAFT
• 00192896042513: SONTEC EAR RASPATORY SERRATED CURVED LEFT SHAFT