Endoscrub®

GUDID 00681490046039

FOOTSWITCH 1852000 ENDO-SCRUB 2

MEDTRONIC XOMED, INC.

Foot-switch, electrical
Primary Device ID00681490046039
NIH Device Record Key65a6efb4-1113-448b-b3c1-2f435939491a
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndoscrub®
Version Model Number1852000
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100681490046039 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EOBNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-29

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