DRILL TUBE 1103-16827

GUDID 00192896093812

DRILL TUBE

SONTEC INSTRUMENTS, INC.

Surgical drill guide, reusable

• Primary Device ID: 00192896093812
• NIH Device Record Key: 1a6782de-2a1b-4dad-a956-f116d0c23525
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRILL TUBE
• Version Model Number: 1103-16827
• Catalog Number: 1103-16827
• 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

• Length: 2.7 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896093812 [Primary]

FDA Product Code

• LXI: Guide, drill, ligament

Sterilization

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

[00192896093812]

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: 2019-03-15
• Device Publish Date: 2019-03-07

On-Brand Devices [DRILL TUBE]

• 00192896096059: DRILL TUBE
• 00192896093829: DRILL TUBE
• 00192896093812: DRILL TUBE