Quadcut

GUDID 00763000579227

BLADE 1884006EM RAD40 4MM M4 ROTATE ROHS

MEDTRONIC XOMED, INC.

Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use Metal/carbide ENT bur, single-use
Primary Device ID00763000579227
NIH Device Record Keyab876696-0835-496b-8ebb-4e00dff5d78c
Commercial Distribution StatusIn Commercial Distribution
Brand NameQuadcut
Version Model Number1884006EM
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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 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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000579227 [Primary]

FDA Product Code

HAWNeurological stereotaxic Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-01-28
Device Publish Date2022-01-20

On-Brand Devices [Quadcut]

00763000579272BLADE 1884380EM QUADCUT 4.3MMX13CM ROHS
00763000579265BLADE 1883480EM QUADCUT 3.4MMX13CM ROHS
00763000579241BLADE 1884080EM TRICUT 4MMX13CM M4 ROHS
00763000579234BLADE 1884012EM RAD12 4MM M4 ROTATE ROHS
00763000579227BLADE 1884006EM RAD40 4MM M4 ROTATE ROHS

Trademark Results [Quadcut]

Mark Image

Registration | Serial
Company
Trademark
Application Date
QUADCUT
QUADCUT
85067363 3942261 Live/Registered
Medtronic Xomed, Inc.
2010-06-21

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