DRILL GUIDE

GUDID 00192896102033

DOUBLE DRILL GUIDE

SONTEC INSTRUMENTS, INC.

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable

Primary Device ID	00192896102033
NIH Device Record Key	199518b6-94ec-4b0d-99a2-3e776588e81e
Commercial Distribution Status	In Commercial Distribution
Brand Name	DRILL GUIDE
Version Model Number	1103-1624
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

Device Dimensions

Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
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Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896102033 [Primary]

FDA Product Code

LXI	Guide, drill, ligament