HEANEY-BALLENTINE FORCEPS 525-434

GUDID 00192896045934

HEANEY-BALLENTINE FORCEPS LONGITUDINAL SERRATED STRAIGHT JAW

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID00192896045934
NIH Device Record Key1451fe71-63d6-482d-9848-ce888464c895
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEANEY-BALLENTINE FORCEPS
Version Model Number525-434
Catalog Number525-434
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 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
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

Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch
Length8.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896045934 [Primary]

FDA Product Code

HFBFORCEPS, BIOPSY, GYNECOLOGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896045934]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-08-21
Device Publish Date2018-09-14

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