FOERSTER SPONGE FORCEPS

GUDID 00192896101265

FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW

SONTEC INSTRUMENTS, INC.

Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable Dressing/utility forceps, scissors-like, reusable
Primary Device ID00192896101265
NIH Device Record Keydf85db3d-d5e1-4ef5-8dac-66eb633ab94a
Commercial Distribution StatusIn Commercial Distribution
Brand NameFOERSTER SPONGE FORCEPS
Version Model Number123-606Q
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 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

Device Dimensions

Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch
Length9.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896101265 [Primary]

FDA Product Code

HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101265]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-28
Device Publish Date2020-04-20

On-Brand Devices [FOERSTER SPONGE FORCEPS]

00192896093164FOERSTER SPONGE FORCEPS STRAIGHT SERRATED TIP
00192896075726FOERSTER SPONGE FORCEPS STRAIGHT SERRATED TIP
00192896021631FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW
00192896021624FOERSTER SPONGE FORCEPS CURVED SERRATED JAW
00192896021617FOERSTER SPONGE FORCEPS CURVED SERRATED JAW
00192896021600FOERSTER SPONGE FORCEPS CURVED SERRATED JAW
00192896021594FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW
00192896021587FOERSTER SPONGE FORCEPS STRAIGHT SMOOTH JAW
00192896021570FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW
00192896021563FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW
00192896021556FOERSTER SPONGE FORCEPS STRAIGHT SMOOTH JAW
00192896101265FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW
00192896105140Foerster Sponge Forceps Curved Serrated Jaw
00192896105911Foerster Sponge Forceps Curved Serrated Jaw

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.