EGRESS CANNULA SC94-0313

GUDID 00192896087804

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 ID00192896087804
NIH Device Record Key3ab46c90-f9c3-4ab8-bff4-4070f61ad791
Commercial Distribution StatusIn Commercial Distribution
Brand NameEGRESS CANNULA
Version Model NumberSC94-0313
Catalog NumberSC94-0313
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0
Lumen/Inner Diameter6 Inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896087804 [Primary]

FDA Product Code

GEACANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-22
Device Publish Date2018-09-21

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00192896087804EGRESS CANNULA WITH CONICAL OBTURATOR
00192896070608EGRESS CANNULA WITH CONICAL OBTURATOR
00192896070592EGRESS CANNULA WITH CONICAL OBTURATOR
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00192896104730Egress Cannula With Conical Obturator 8.1 Millimeter Inner Diameter
00192896110830Egress Cannula With Conical Obturator 7.1 Millimeter Inner Diameter
00192896110984Egress Cannula With Conical Obturator
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