ETHMOID FORCEPS 1404-783

GUDID 00192896058767

ETHMOID FORCEPS UP-ANGLE TIPS

SONTEC INSTRUMENTS, INC.

Bone holding forceps
Primary Device ID00192896058767
NIH Device Record Key89caef82-ff39-4437-94e7-c280de93085f
Commercial Distribution StatusIn Commercial Distribution
Brand NameETHMOID FORCEPS
Version Model Number1404-783
Catalog Number1404-783
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does n
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896058767 [Primary]

FDA Product Code

KAEFORCEPS, ENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896058767]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-29
Device Publish Date2018-09-27

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