EGRESS CANNULA SC94-0319

GUDID 00192896070608

EGRESS CANNULA WITH CONICAL OBTURATOR

SONTEC INSTRUMENTS, INC.

Suction cannula, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable

Primary Device ID	00192896070608
NIH Device Record Key	c3275f29-a3fd-4b84-b678-c2052a4b8a94
Commercial Distribution Status	In Commercial Distribution
Brand Name	EGRESS CANNULA
Version Model Number	SC94-0319
Catalog Number	SC94-0319
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
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	12 Inch
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch
Lumen/Inner Diameter	6.1 Millimeter
Length	12 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896070608 [Primary]

FDA Product Code

GEA	CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY