BARR PROBE 508-547

GUDID 00192896044661

BARR PROBE DOUBLE ENDED

SONTEC INSTRUMENTS, INC.

Rectal probe
Primary Device ID00192896044661
NIH Device Record Key76c7355c-e01b-4899-9960-bc0542cc9887
Commercial Distribution StatusIn Commercial Distribution
Brand NameBARR PROBE
Version Model Number508-547
Catalog Number508-547
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

Device Dimensions

Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896044661 [Primary]

FDA Product Code

HXBPROBE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044661]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-15
Device Publish Date2018-09-14

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