MatrixMIDFACE 03503148

GUDID H980035031480

MATRIXMIDFACE 1.25MM DRILL BIT MQC/18MM STOP/44.5MM

SYNTHES (U.S.A.) LP

Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable
Primary Device IDH980035031480
NIH Device Record Keye81731aa-5afa-49d0-9619-e904ac9312ce
Commercial Distribution StatusIn Commercial Distribution
Brand NameMatrixMIDFACE
Version Model Number03.503.148
Catalog Number03503148
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
Device Count1
DM Exempttrue
Pre-market Exemptfalse
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)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110887587012186 [Primary]
HIBCCH980035031480 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZIDRILL, BONE, POWERED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


[H980035031480]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-11-22
Device Publish Date2018-09-21

On-Brand Devices [MatrixMIDFACE]

20887587019557TI MATRIXMIDFACE EMERGENCY SCREW 18MM
20887587019540TI MATRIXMIDFACE EMERGENCY SCREW 18MM
20887587019519TI MATRIXMIDFACE EMERGENCY SCREW 16MM
20887587019502TI MATRIXMIDFACE EMERGENCY SCREW 16MM
20887587019472TI MATRIXMIDFACE EMERGENCY SCREW 14MM
20887587019465TI MATRIXMIDFACE EMERGENCY SCREW 14MM
20887587019434TI MATRIXMIDFACE EMERGENCY SCREW 12MM
20887587019427TI MATRIXMIDFACE EMERGENCY SCREW 12MM
20887587019403TI MATRIXMIDFACE EMERGENCY SCREW 10MM
20887587019397TI MATRIXMIDFACE EMERGENCY SCREW 10MM
20887587019373TI MATRIXMIDFACE EMERGENCY SCREW 8MM
20887587019366TI MATRIXMIDFACE EMERGENCY SCREW 8MM
20887587019342TI MATRIXMIDFACE EMERGENCY SCREW 6MM
20887587019335TI MATRIXMIDFACE EMERGENCY SCREW 6MM
20887587019311TI MATRIXMIDFACE EMERGENCY SCREW 5MM
20887587019304TI MATRIXMIDFACE EMERGENCY SCREW 5MM
20887587019281TI MATRIXMIDFACE EMERGENCY SCREW 4MM
20887587019274TI MATRIXMIDFACE EMERGENCY SCREW 4MM
20887587019250TI MATRIXMIDFACE EMERGENCY SCREW 3MM
20887587019243TI MATRIXMIDFACE EMERGENCY SCREW 3MM
20887587019229TI MATRIXMIDFACE SCREW SELF-DRILLING 8MM
20887587019212TI MATRIXMIDFACE SCREW SELF-DRILLING 8MM
20887587019199TI MATRIXMIDFACE SCREW SELF-DRILLING 6MM
20887587019182TI MATRIXMIDFACE SCREW SELF-DRILLING 6MM
20887587019168TI MATRIXMIDFACE SCREW SELF-DRILLING 5MM
20887587019151TI MATRIXMIDFACE SCREW SELF-DRILLING 5MM
20887587019137TI MATRIXMIDFACE SCREW SELF-DRILLING 4MM
20887587019120TI MATRIXMIDFACE SCREW SELF-DRILLING 4MM
20887587019106TI MATRIXMIDFACE SCREW SELF-DRILLING 3MM
20887587019090TI MATRIXMIDFACE SCREW SELF-DRILLING 3MM
20887587019076TI MATRIXMIDFACE SCREW SELF-TAPPING 18MM
20887587019069TI MATRIXMIDFACE SCREW SELF-TAPPING 18MM
20887587019021TI MATRIXMIDFACE SCREW SELF-TAPPING 16MM
20887587019014TI MATRIXMIDFACE SCREW SELF-TAPPING 16MM
20887587018970TI MATRIXMIDFACE SCREW SELF-TAPPING 14MM
20887587018963TI MATRIXMIDFACE SCREW SELF-TAPPING 14MM
20887587018925TI MATRIXMIDFACE SCREW SELF-TAPPING 12MM
20887587018918TI MATRIXMIDFACE SCREW SELF-TAPPING 12MM
20887587018895TI MATRIXMIDFACE SCREW SELF-TAPPING 10MM
20887587018888TI MATRIXMIDFACE SCREW SELF-TAPPING 10MM
20887587018864TI MATRIXMIDFACE SCREW SELF-TAPPING 8MM
20887587018857TI MATRIXMIDFACE SCREW SELF-TAPPING 8MM
20887587018833TI MATRIXMIDFACE SCREW SELF-TAPPING 6MM
20887587018826TI MATRIXMIDFACE SCREW SELF-TAPPING 6MM
20887587018802TI MATRIXMIDFACE SCREW SELF-TAPPING 5MM
20887587018796TI MATRIXMIDFACE SCREW SELF-TAPPING 5MM
20887587018772TI MATRIXMIDFACE SCREW SELF-TAPPING 4MM
20887587018765TI MATRIXMIDFACE SCREW SELF-TAPPING 4MM
20887587018741TI MATRIXMIDFACE SCREW SELF-TAPPING 3MM
20887587018734TI MATRIXMIDFACE SCREW SELF-TAPPING 3MM

Trademark Results [MatrixMIDFACE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MATRIXMIDFACE
MATRIXMIDFACE
87315654 5394395 Live/Registered
DePuy Synthes, Inc.
2017-01-27

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