POWEREASE™ Instruments

GUDID 00613994952066

DRILL BIT G2345030M 3.0MM DRILL BIT

MEDTRONIC SOFAMOR DANEK, INC.

Fluted surgical drill bit, single-use, sterile
Primary Device ID00613994952066
NIH Device Record Key8bfb0c28-95a4-4dda-bbeb-24f7d944b7d5
Commercial Distribution StatusIn Commercial Distribution
Brand NamePOWEREASE™ Instruments
Version Model NumberG2345030M
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, 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 Perscriptionfalse
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 Dimensions

Device Size Text, specify0
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Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100613994952066 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HBEDRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-11-22
Device Publish Date2016-04-16

On-Brand Devices [POWEREASE™ Instruments]

00613994952073DRILL BIT G2345030S 3.0MM DRILL BIT
00613994952066DRILL BIT G2345030M 3.0MM DRILL BIT
00613994952059DRILL BIT G2345030L 3.0MM DRILL BIT
00613994952042DRILL BIT G2345035S 3.5MM DRILL BIT
00613994952035DRILL BIT G2345035M 3.5MM DRILL BIT
00613994952028DRILL BIT G2345035L 3.5MM DRILL BIT
00613994952011DRILL BIT G2345042S 4.2MM DRILL BIT
00613994952004DRILL BIT G2345042M 4.2MM DRILL BIT
00613994951991DRILL BIT G2345042L 4.2MM DRILL BIT
00613994917713ROD CUTTER 2346030 ROD CUTTER
00613994917706COUNTER TORQUE 2346013 5.5 OFFSET
00613994917690COUNTER TORQUE 2346012 5.5/6.0 MAS/FAS
00613994917683COUNTER TORQUE 2346011 4.75 MAS/FAS
00613994917676BREAKOFF 2346010 SET SCREW BREAKOFF
00613994917652DRILL BIT 2345042L 4.2MM DRILL BIT
00613994917645DRILL BIT 2345042M 4.2MM DRILL BIT
00613994917638DRILL BIT 2345042S 4.2MM DRILL BIT
00613994917621DRILL BIT 2345035L 3.5MM DRILL BIT
00613994917614DRILL BIT 2345035M 3.5MM DRILL BIT
00613994917607DRILL BIT 2345035S 3.5MM DRILL BIT
00613994917591DRILL BIT 2345030L 3.0MM DRILL BIT
00613994917584DRILL BIT 2345030M 3.0MM DRILL BIT
00613994917577DRILL BIT 2345030S 3.0MM DRILL BIT
00613994917539TRAY 2397002 POWEREASE HANDPIECE
00613994907592CABLE 2344000 POWEREASE NIM
00613994907448CONSOLE 2340000 POWEREASE IPC
00613994905734POST CUTTER 2346020 POST CUTTER
00613994905727SCREWDRIVER 2342306M 5.5 MAS
00613994905710SCREWDRIVER 2342306L 5.5 MAS
00613994905703SCREWDRIVER 2342305S 4.75 MAS
00613994905697SCREWDRIVER 2342305M 4.75 MAS
00613994905680SCREWDRIVER 2342305L 4.75 MAS
00613994905673SCREWDRIVER 2342301S 5.5 RMAS
00613994905666SCREWDRIVER 2342301M 5.5 RMAS
00613994905659SCREWDRIVER 2342301L 5.5 RMAS
00613994905642SCREWDRIVER 2342300S 4.75 RMAS
00613994905635SCREWDRIVER 2342300M 4.75 RMAS
00613994905628SCREWDRIVER 2342300L 4.75 RMAS
00613994905611SCREWDRIVER 2342281S 5.5 FAS
00613994905604SCREWDRIVER 2342281M 5.5 FAS
00613994905598SCREWDRIVER 2342281L 5.5 FAS
00613994905581SCREWDRIVER 2342306S 5.5 MAS
00613994905574SLEEVE 2343431S 9.0MM NIM SLEEVE
00613994905567SLEEVE 2343431M 9.0MM NIM SLEEVE
00613994905550SLEEVE 2343431L 9.0MM NIM SLEEVE
00613994905543SLEEVE 2343429S 8.0MM NIM SLEEVE
00613994905536SLEEVE 2343429M 8.0MM NIM SLEEVE
00613994905529SLEEVE 2343429L 8.0MM NIM SLEEVE
00613994905512SLEEVE 2343426S 6.5MM NIM SLEEVE
00613994905505SLEEVE 2343426M 6.5MM NIM SLEEVE

Trademark Results [POWEREASE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
POWEREASE
POWEREASE
90523662 not registered Live/Pending
BISSELL Inc.
2021-02-10
POWEREASE
POWEREASE
78940823 3645073 Dead/Cancelled
ACCO Brands Corporation
2006-07-31
POWEREASE
POWEREASE
77899385 3833047 Live/Registered
BISSELL Homecare, Inc.
2009-12-22
POWEREASE
POWEREASE
77547033 4139366 Live/Registered
Warsaw Orthopedic, Inc.
2008-08-14
POWEREASE
POWEREASE
75248539 2130605 Live/Registered
Life Technologies Corporation
1997-02-27
POWEREASE
POWEREASE
74687135 not registered Dead/Abandoned
Novel Experimental Technology
1995-06-12

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