Fomon Nasal Rasp 345-355

GUDID 00192896118379

Fomon Nasal Rasp Double-Ended With Diamond Coating

SONTEC INSTRUMENTS, INC.

Nasal file/rasp
Primary Device ID00192896118379
NIH Device Record Key145ab4e0-9687-4426-bbcd-57a81f888ba5
Commercial Distribution StatusIn Commercial Distribution
Brand NameFomon Nasal Rasp
Version Model Number345-355
Catalog Number345-355
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

Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter
Length21 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896118379 [Primary]

FDA Product Code

KBARASP, NASAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

[00192896118379]

Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-08-15
Device Publish Date2024-08-07

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