JANSEN MIDDLETON SEPTUM FORCEPS 475-352

GUDID 00192896092532

JANSEN MIDDLETON SEPTUM FORCEPS CUT THRU

SONTEC INSTRUMENTS, INC.

Nasal scissors

• Primary Device ID: 00192896092532
• NIH Device Record Key: bdadfb8a-b196-409b-8e5c-fc0bc5510b5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JANSEN MIDDLETON SEPTUM FORCEPS
• Version Model Number: 475-352
• Catalog Number: 475-352
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896092532 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[00192896092532]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-04
• Device Publish Date: 2019-01-03

On-Brand Devices [JANSEN MIDDLETON SEPTUM FORCEPS]

• 00192896092556: JANSEN MIDDLETON SEPTUM FORCEPS
• 00192896092532: JANSEN MIDDLETON SEPTUM FORCEPS CUT THRU