SONTEC MICRO RASPATORY 345-267

GUDID 00192896078338

SONTEC MICRO RASPATORY SINGLE ENDED/SIDED EXTRA NECK

SONTEC INSTRUMENTS, INC.

Nasal file/rasp
Primary Device ID00192896078338
NIH Device Record Key1c17a17f-2f9d-4be6-aa0a-5855ae2aafff
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC MICRO RASPATORY
Version Model Number345-267
Catalog Number345-267
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

Device Dimensions

Length7 Inch
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch
Device Size Text, specify0
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896078338 [Primary]

FDA Product Code

KBARASP, NASAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896078338]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-05-01
Device Publish Date2018-09-20

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