ENDOLARYNGEAL ELEVATOR 1301-530

GUDID 00192896058750

ENDOLARYNGEAL ELEVATOR MICROSCOPIC SLIGHT CURVED BLUNT TIP

SONTEC INSTRUMENTS, INC.

ENT elevator
Primary Device ID00192896058750
NIH Device Record Keycc99a21c-bb73-41a3-88b8-873be0012aa9
Commercial Distribution StatusIn Commercial Distribution
Brand NameENDOLARYNGEAL ELEVATOR
Version Model Number1301-530
Catalog Number1301-530
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

Length9.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896058750 [Primary]

FDA Product Code

KADELEVATOR, ENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896058750]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-07-12
Device Publish Date2018-09-27

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