GROOVED RASPATORY 1103-379

GUDID 00192896052918

GROOVED RASPATORY FINE GRIT CURVED TIP DIAMOND COATED

SONTEC INSTRUMENTS, INC.

Bone file/rasp, manual Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable Bone file/rasp, manual, reusable

• Primary Device ID: 00192896052918
• NIH Device Record Key: 7302f615-dda7-45cd-b86f-1944a912624e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GROOVED RASPATORY
• Version Model Number: 1103-379
• Catalog Number: 1103-379
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 7.5 Inch
• Length: 7.5 Inch
• Device Size Text, specify: 0
• Length: 7.5 Inch
• Device Size Text, specify: 0
• Length: 7.5 Inch
• Device Size Text, specify: 0
• Length: 7.5 Inch
• Device Size Text, specify: 0
• Length: 7.5 Inch
• Device Size Text, specify: 0
• Length: 7.5 Inch
• Device Size Text, specify: 0
• Length: 7.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896052918 [Primary]

FDA Product Code

• HTR: Rasp

Sterilization

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

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896052918]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-06-12
• Device Publish Date: 2018-10-09

On-Brand Devices [GROOVED RASPATORY ]

• 00192896082977: GROOVED RASPATORY MEDIUM GRIT CURVED TIP DIAMOND COATED
• 00192896082960: GROOVED RASPATORY MEDIUM GRIT CURVED TIP DIAMOND COATED
• 00192896082953: GROOVED RASPATORY FINE GRIT CURVED TIP DIAMOND COATED
• 00192896052918: GROOVED RASPATORY FINE GRIT CURVED TIP DIAMOND COATED