Canal Finder Raspatory 345-223

GUDID 00192896120730

Canal Finder Raspatory With Silicone Handle Curved

SONTEC INSTRUMENTS, INC.

Bone file/rasp, manual, reusable

• Primary Device ID: 00192896120730
• NIH Device Record Key: ccdf5ba7-bf06-4feb-aa33-e88c36ba4313
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Canal Finder Raspatory
• Version Model Number: 345-223
• Catalog Number: 345-223
• 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
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch
• Length: 8 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896120730 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

[00192896120730]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-04
• Device Publish Date: 2024-10-25

On-Brand Devices [Canal Finder Raspatory]

• 00192896120747: Canal Finder Raspatory With Silicone Handle Straight
• 00192896120730: Canal Finder Raspatory With Silicone Handle Curved