Black Bipolar Gerald Bayonet Forceps

GUDID 00192896112162

Black Bipolar Gerald Bayonet Forceps Non-Stick Insulated

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Primary Device ID00192896112162
NIH Device Record Key53417f9c-d0cc-4a1d-92f1-8511fad0f8f9
Commercial Distribution StatusIn Commercial Distribution
Brand NameBlack Bipolar Gerald Bayonet Forceps
Version Model Number2700-990NS
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Latextrue
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

Device Dimensions

Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch
Device Size Text, specify0
Length7.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896112162 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, cutting & coagulation & accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896112162]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-31
Device Publish Date2021-12-23

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