Lemmon Sternal Spreader 2500-145

GUDID 00192896121034

Lemmon Sternal Spreader Serrated

SONTEC INSTRUMENTS, INC.

Rib spreader, reusable
Primary Device ID00192896121034
NIH Device Record Key600e3ddc-ebaa-446d-9d8f-f049b7de62d6
Commercial Distribution StatusIn Commercial Distribution
Brand NameLemmon Sternal Spreader
Version Model Number2500-145
Catalog Number2500-145
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896121034 [Primary]

FDA Product Code

GADRETRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896121034]

Dry Heat Sterilization


[00192896121034]

Dry Heat Sterilization


[00192896121034]

Dry Heat Sterilization


[00192896121034]

Dry Heat Sterilization


[00192896121034]

Dry Heat Sterilization


[00192896121034]

Dry Heat Sterilization


[00192896121034]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-14
Device Publish Date2025-01-06

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