Canal Finder Raspatory 345-221

GUDID 00192896120747

Canal Finder Raspatory With Silicone Handle Straight

SONTEC INSTRUMENTS, INC.

Bone file/rasp, manual, reusable
Primary Device ID00192896120747
NIH Device Record Key2390e8f6-db74-4a7a-83fc-cd6740e9ed3b
Commercial Distribution StatusIn Commercial Distribution
Brand NameCanal Finder Raspatory
Version Model Number345-221
Catalog Number345-221
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

Device Dimensions

Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896120747 [Primary]

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


[00192896120747]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-04
Device Publish Date2024-10-25

On-Brand Devices [Canal Finder Raspatory]

00192896120747Canal Finder Raspatory With Silicone Handle Straight
00192896120730Canal Finder Raspatory With Silicone Handle Curved

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