SONTEC BONE HOOK 320-930

GUDID 00192896029262

SONTEC BONE HOOK MEDIUM

SONTEC INSTRUMENTS, INC.

Bone hook

• Primary Device ID: 00192896029262
• NIH Device Record Key: 79d55426-7d1f-46a1-a845-91fd43d1e21f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONTEC BONE HOOK
• Version Model Number: 320-930
• Catalog Number: 320-930
• 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: 9 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896029262 [Primary]

FDA Product Code

• KIK: HOOK, BONE

Sterilization

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

[00192896029262]

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: 2018-11-05
• Device Publish Date: 2018-10-04

On-Brand Devices [SONTEC BONE HOOK]

• 00192896029279: SONTEC BONE HOOK LARGE
• 00192896029262: SONTEC BONE HOOK MEDIUM
• 00192896029255: SONTEC BONE HOOK SMALL