MOLT PERIOSTEAL ELEVATOR 1103-337

GUDID 00192896052819

MOLT PERIOSTEAL ELEVATOR #MX2/4 DOUBLE ENDED BLADE

SONTEC INSTRUMENTS, INC.

Periosteal elevator, reusable
Primary Device ID00192896052819
NIH Device Record Key3defd748-c631-41e0-baf3-00f742151796
Commercial Distribution StatusIn Commercial Distribution
Brand NameMOLT PERIOSTEAL ELEVATOR
Version Model Number1103-337
Catalog Number1103-337
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896052819 [Primary]

FDA Product Code

EMJElevator, Surgical, Dental
EMKCURETTE, SURGICAL, DENTAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896052819]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-09-17
Device Publish Date2018-09-24

On-Brand Devices [MOLT PERIOSTEAL ELEVATOR]

00192896082908MOLT PERIOSTEAL ELEVATOR SINGLE ENDED TIP #EX-6
00192896053229MOLT PERIOSTEAL ELEVATOR #CS M-9
00192896052819MOLT PERIOSTEAL ELEVATOR #MX2/4 DOUBLE ENDED BLADE
00192896093928MOLT PERIOSTEAL ELEVATOR DOUBLE ENDED TIPS #EX-1

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