DRILL TUBE 1103-16820

GUDID 00192896096059

DRILL TUBE

SONTEC INSTRUMENTS, INC.

Surgical drill guide, reusable

• Primary Device ID: 00192896096059
• NIH Device Record Key: 4fc8203c-fc4b-4970-8d5a-72154346ff08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRILL TUBE
• Version Model Number: 1103-16820
• Catalog Number: 1103-16820
• 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: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896096059 [Primary]

FDA Product Code

• LXI: Guide, Drill, Ligament

Sterilization

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

[00192896096059]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-06-04
• Device Publish Date: 2019-05-08

On-Brand Devices [DRILL TUBE]

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