BONE RASPATORY 1100-488

GUDID 00192896081468

BONE RASPATORY DOUBLE ENDED TIPS #772

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	00192896081468
NIH Device Record Key	17a0aeb0-6749-43da-95a9-62f9f38b00b7
Commercial Distribution Status	In Commercial Distribution
Brand Name	BONE RASPATORY
Version Model Number	1100-488
Catalog Number	1100-488
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

Device Dimensions

Length	7 Inch
Length	7 Inch
Length	7 Inch
Length	7 Inch
Length	7 Inch
Length	7 Inch
Length	7 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896081468 [Primary]

FDA Product Code

KBA	RASP, NASAL