ROSS VENTRICULAR VENT TUBE

GUDID B09927003950

ROSS VENTRICULAR VENT ADULT TUBE

SONTEC INSTRUMENTS, INC.

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

Primary Device ID	B09927003950
NIH Device Record Key	16ed0b7b-f0b4-49aa-9ff6-77a8c1cf94f8
Commercial Distribution Status	In Commercial Distribution
Brand Name	ROSS VENTRICULAR VENT TUBE
Version Model Number	2700-395
Company DUNS	040729840
Company Name	SONTEC INSTRUMENTS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com
Phone	18008217496
Email	info@sontecinstruments.com

Device Dimensions

Length	0.1875 Inch
Length	0.1875 Inch
Length	0.1875 Inch
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	51 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896006102 [Primary]
HIBCC	B09927003950 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K152400

FDA Product Code

GCJ	Laparoscope, General & Plastic Surgery