NIM CONTACT®

GUDID 00643169789555

EMG TUBE 8229506 NIM CONT 6MM ROHS

MEDTRONIC XOMED, INC.

Basic endotracheal tube, single-use
Primary Device ID00643169789555
NIH Device Record Key0999de87-e2fb-4d4d-9c46-64bbfb9926bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameNIM CONTACT®
Version Model Number8229506
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 Usetrue
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)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Outer Diameter9 Millimeter
Outer Diameter9 Millimeter
Outer Diameter9 Millimeter
Outer Diameter9 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169789555 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETNSTIMULATOR, NERVE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-11-06

On-Brand Devices [NIM CONTACT®]

00643169789579EMG TUBE 8229508 NIM CONT 8MM ROHS
00643169789562EMG TUBE 8229507 NIM CONT 7MM ROHS
00643169789555EMG TUBE 8229506 NIM CONT 6MM ROHS
00643169358775ENDOTRACH TUBE 8229508 CONT EMG 8MM ROHS
00643169358768ENDOTRACH TUBE 8229507 CONT EMG 7MM ROHS
00643169358751ENDOTRACH TUBE 8229506 CONT EMG 6MM ROHS

Trademark Results [NIM CONTACT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NIM CONTACT
NIM CONTACT
78600100 3276757 Live/Registered
Medtronic Xomed, Inc.
2005-04-01

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.