FERRIS SMITH WILDE RONGEUR 404-777

GUDID 00192896092617

FERRIS SMITH WILDE RONGEUR STRAIGHT TIP

SONTEC INSTRUMENTS, INC.

Orthopaedic joint/limb rongeur
Primary Device ID00192896092617
NIH Device Record Key40e0bcc1-e5ed-46d0-8d2e-2eb2ec6f395b
Commercial Distribution StatusIn Commercial Distribution
Brand NameFERRIS SMITH WILDE RONGEUR
Version Model Number404-777
Catalog Number404-777
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

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896092617 [Primary]

FDA Product Code

HTXRONGEUR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896092617]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-07-12
Device Publish Date2019-01-03

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