LUMBAR/CERVICAL IMPACTOR 335-396

GUDID 00192896031371

LUMBAR/CERVICAL IMPACTOR MICROSCOPIC LATERAL OFFSET

SONTEC INSTRUMENTS, INC.

Bone trephine

• Primary Device ID: 00192896031371
• NIH Device Record Key: 04765f21-3483-4648-942d-d890b619b4e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUMBAR/CERVICAL IMPACTOR
• Version Model Number: 335-396
• Catalog Number: 335-396
• 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
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0
• Length: 8.5 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896031371 [Primary]

FDA Product Code

• HWA: IMPACTOR

Sterilization

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

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896031371]

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: 2018-10-15
• Device Publish Date: 2018-09-12

On-Brand Devices [LUMBAR/CERVICAL IMPACTOR]

• 00192896031401: LUMBAR/CERVICAL IMPACTOR WIDE LATERAL
• 00192896031395: LUMBAR/CERVICAL IMPACTOR WIDE LATERAL
• 00192896031388: LUMBAR/CERVICAL IMPACTOR GUARDED MICROSCOPIC LATERAL
• 00192896031371: LUMBAR/CERVICAL IMPACTOR MICROSCOPIC LATERAL OFFSET
• 00192896031364: LUMBAR/CERVICAL IMPACTOR MICRO LATERAL OFFSET WITH HEEL
• 00192896031357: LUMBAR/CERVICAL IMPACTOR MICRO LATERAL OFFSET WITHOUT HEEL
• 00192896031340: LUMBAR/CERVICAL IMPACTOR LATERAL NARROW TIPS
• 00192896031333: LUMBAR/CERVICAL IMPACTOR