SMITH PETERSEN OSTEOTOME 330-623

GUDID 00192896094444

SMITH PETERSEN OSTEOTOME CURVED BLADE

SONTEC INSTRUMENTS, INC.

Orthopaedic osteotome

• Primary Device ID: 00192896094444
• NIH Device Record Key: 482fa063-bb47-44f4-9a00-474c79e67c76
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SMITH PETERSEN OSTEOTOME
• Version Model Number: 330-623
• Catalog Number: 330-623
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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: 8 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896094444 [Primary]

FDA Product Code

• HWM: OSTEOTOME

Sterilization

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

[00192896094444]

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 [SMITH PETERSEN OSTEOTOME]

• 00192896094444: SMITH PETERSEN OSTEOTOME CURVED BLADE
• 00192896101432: SMITH PETERSEN OSTEOTOME CURVED