ROSS SUMP SUCKER

GUDID B09927003900

ROSS SUMP SUCKER ADULT

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	B09927003900
NIH Device Record Key	bf7e47eb-06a5-475b-8cf4-673f84fb9aa2
Commercial Distribution Status	In Commercial Distribution
Brand Name	ROSS SUMP SUCKER
Version Model Number	2700-390
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	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
Email	INFO@SONTECINSTRUMENTS.COM
Phone	8008217496
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
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter
Device Size Text, specify	0
Outer Diameter	7.5 Millimeter
Length	43 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896006072 [Primary]
HIBCC	B09927003900 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K152400

FDA Product Code

GCJ	Laparoscope, General & Plastic Surgery