SMITH PETERSEN OSTEOTOME

GUDID 00192896101432

SMITH PETERSEN OSTEOTOME CURVED

SONTEC INSTRUMENTS, INC.

Orthopaedic osteotome Orthopaedic osteotome Orthopaedic osteotome
Primary Device ID00192896101432
NIH Device Record Key108ffbe5-c71b-455d-85b6-d3b651e4bb27
Commercial Distribution StatusIn Commercial Distribution
Brand NameSMITH PETERSEN OSTEOTOME
Version Model Number330-626
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

Device Dimensions

Device Size Text, specify0
Length8 Inch
Device Size Text, specify0
Length8 Inch
Device Size Text, specify0
Length8 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896101432 [Primary]
GS100192896101432 [Primary]
GS100192896101432 [Primary]

FDA Product Code

HWMOSTEOTOME
HWMOSTEOTOME
HWMOSTEOTOME

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896101432]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896101432]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896101432]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-19
Device Publish Date2020-05-11

On-Brand Devices [SMITH PETERSEN OSTEOTOME]

00192896094444SMITH PETERSEN OSTEOTOME CURVED BLADE
00192896101432SMITH PETERSEN OSTEOTOME CURVED

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