CANNULA-IRRIGATION SET SC95-0415-SET

GUDID 00192896093201

CANNULA-IRRIGATION SET WITH STOPCOCK & SHARP/BLUNT OBTURATOR

SONTEC INSTRUMENTS, INC.

Surgical drill guide obturator
Primary Device ID00192896093201
NIH Device Record Key59d9f76d-d6ef-4228-aa80-e1192ee2d48e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCANNULA-IRRIGATION SET
Version Model NumberSC95-0415-SET
Catalog NumberSC95-0415-SET
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
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter
Length4.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896093201 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896093201]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-02-04
Device Publish Date2019-01-03

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