SONTEC STIFLE THRUST LEVER 1100-6691

GUDID 00192896049383

SONTEC STIFLE THRUST LEVER

SONTEC INSTRUMENTS, INC.

Nerve/vessel retractor
Primary Device ID00192896049383
NIH Device Record Key3ff036ba-f9f6-4cba-b052-8970d870d22f
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC STIFLE THRUST LEVER
Version Model Number1100-6691
Catalog Number1100-6691
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

Length8.375 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896049383 [Primary]

FDA Product Code

EIGRETRACTOR, ALL TYPES
GADRetractor

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896049383]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-22
Device Publish Date2018-09-14

On-Brand Devices [SONTEC STIFLE THRUST LEVER]

00192896081932SONTEC STIFLE THRUST LEVER
00192896049383SONTEC STIFLE THRUST LEVER

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