SONTEC SUCTION TUBE

GUDID B0991804440

SONTEC SUCTION TUBE WITH FINGER CONTROL

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	B0991804440
NIH Device Record Key	27157ced-f7a2-44d6-b2e5-c9f6faeac07b
Commercial Distribution Status	In Commercial Distribution
Brand Name	SONTEC SUCTION TUBE
Version Model Number	180-444
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	+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	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0
Length	18 Inch
Device Size Text, specify	0
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896000568 [Primary]
HIBCC	B0991804440 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K152400

FDA Product Code

GCJ	Laparoscope, General & Plastic Surgery
JOL	Catheter And Tip, Suction

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[B0991804440]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804440]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804440]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804440]