PITANGUY OSTEOTOME 475-719

GUDID 00192896042629

PITANGUY OSTEOTOME SEMI GUARDED U-SHAPED TIP

SONTEC INSTRUMENTS, INC.

Orthopaedic chisel
Primary Device ID00192896042629
NIH Device Record Keyeb20a337-b8d4-4830-90a4-1ee5c28ae4f7
Commercial Distribution StatusIn Commercial Distribution
Brand NamePITANGUY OSTEOTOME
Version Model Number475-719
Catalog Number475-719
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

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896042629 [Primary]

FDA Product Code

KDGCHISEL (OSTEOTOME)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896042629]

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 Date2018-09-12

On-Brand Devices [PITANGUY OSTEOTOME]

00192896080225PITANGUY OSTEOTOME U-SHAPED SEMI-GUARDED TIP
00192896042636PITANGUY OSTEOTOME SEMI GUARDED U-SHAPED TIP
00192896042629PITANGUY OSTEOTOME SEMI GUARDED U-SHAPED TIP

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.