CLAW CHOPPER T12-1415

GUDID 00192896072558

CLAW CHOPPER SINGLE ENDED TITANIUM

SONTEC INSTRUMENTS, INC.

Eye spud/needle

• Primary Device ID: 00192896072558
• NIH Device Record Key: e616074c-892b-4159-b659-a640cde1501e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLAW CHOPPER
• Version Model Number: T12-1415
• Catalog Number: T12-1415
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00192896072558 [Primary]

FDA Product Code

• HNA: Spud, ophthalmic

Sterilization

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

[00192896072558]

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: 2018-10-22
• Device Publish Date: 2018-09-19

On-Brand Devices [CLAW CHOPPER]

• 00192896072558: CLAW CHOPPER SINGLE ENDED TITANIUM
• 00192896103061: Claw Chopper Single End Stainless Steel