BIPOLAR GERALD BAYONET FORCEPS

GUDID B09927009900

BIPOLAR GERALD BAYONET FORCEPS INSULATED STAINLESS STEEL

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Primary Device IDB09927009900
NIH Device Record Keyd2e1ad52-486d-4c81-b0f3-522a868b6676
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIPOLAR GERALD BAYONET FORCEPS
Version Model Number2700-990
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length7.5 Inch
Length7.5 Inch
Length7.5 Inch
Length7.5 Inch
Length7.5 Inch
Length7.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896006713 [Primary]
HIBCCB09927009900 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09927009900]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B09927009900]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B09927009900]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-24
Device Publish Date2018-08-22

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