Rochester Pean Forceps 115-492Q

GUDID 00192896117587

Rochester Pean Forceps Curved Serrated Tip Quantum

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Primary Device ID00192896117587
NIH Device Record Key6c60c85a-9953-4938-a6bf-9a4a5858e6cb
Commercial Distribution StatusIn Commercial Distribution
Brand NameRochester Pean Forceps
Version Model Number115-492Q
Catalog Number115-492Q
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
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

Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch
Length7.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896117587 [Primary]

FDA Product Code

HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


[00192896117587]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-13
Device Publish Date2024-05-03

On-Brand Devices [Rochester Pean Forceps]

00192896100824ROCHESTER PEAN FORCEPS STRAIGHT SERRATED TIP
00192896117587Rochester Pean Forceps Curved Serrated Tip Quantum

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