Splinter Forceps

GUDID 00192896102583

Carmalt Splinter Forceps Curved Tip

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
Primary Device ID00192896102583
NIH Device Record Key86edae14-557e-4e24-8eff-8102f0398a8a
Commercial Distribution StatusIn Commercial Distribution
Brand NameSplinter Forceps
Version Model Number138-035
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

Device Dimensions

Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch
Length4.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]
GS100192896102583 [Primary]

FDA Product Code

HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS
HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896102583]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-23
Device Publish Date2020-06-15

On-Brand Devices [Splinter Forceps]

00192896023338SPLINTER FORCEPS ANGLED TIP
00192896102583Carmalt Splinter Forceps Curved Tip
00192896102576Feilchenfeld Splinter Forceps

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