Columbus® REVISION NR248K

GUDID 04046963339500

COLUMBUS TIB.HEMI-SPCR.T2/2+ 5MM RL/LM

Aesculap AG

Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge
Primary Device ID04046963339500
NIH Device Record Key21bba763-8ab0-4251-9652-bde7527bddf7
Commercial Distribution StatusIn Commercial Distribution
Brand NameColumbus® REVISION
Version Model NumberNR248K
Catalog NumberNR248K
Company DUNS315018218
Company NameAesculap AG
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104046963339500 [Primary]

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-07-30
Device Publish Date2015-09-24

On-Brand Devices [Columbus® REVISION]

04046963339647COLUMBUS TIB.HEMI-SPCR.T5 15MM RL/LM
04046963339630COLUMBUS TIB.HEMI-SPCR.T5 10MM RL/LM
04046963339623COLUMBUS TIB.HEMI-SPCR.T5 5MM RL/LM
04046963339609COLUMBUS TIB.HEMI-SPCR.T4/4+ 15MM RL/LM
04046963339593COLUMBUS TIB.HEMI-SPCR.T4/4+ 10MM RL/LM
04046963339586COLUMBUS TIB.HEMI-SPCR.T4/4+ 5MM RL/LM
04046963339562COLUMBUS TIB.HEMI-SPCR.T3/3+ 15MM RL/LM
04046963339555COLUMBUS TIB.HEMI-SPCR.T3/3+ 10MM RL/LM
04046963339548COLUMBUS TIB.HEMI-SPCR.T3/3+ 5MM RL/LM
04046963339524COLUMBUS TIB.HEMI-SPCR.T2/2+ 15MM RL/LM
04046963339517COLUMBUS TIB.HEMI-SPCR.T2/2+ 10MM RL/LM
04046963339500COLUMBUS TIB.HEMI-SPCR.T2/2+ 5MM RL/LM
04046963339487COLUMBUS TIB.HEMI-SPCR.T1/1+ 15MM RL/LM
04046963339470COLUMBUS TIB.HEMI-SPCR.T1/1+ 10MM RL/LM
04046963339449COLUMBUS TIB.HEMI-SPCR.T0/0+ 15MM RL/LM
04046963339425COLUMBUS TIB.HEMI-SPCR.T0/0+ 5MM RL/LM
04046963338022COLUMBUS TIB.HEMI-SPCR.T4/4+ 15MM RM/LL
04046963338008COLUMBUS TIB.HEMI-SPCR.T4/4+ 5MM RM/LL
04046963337926COLUMBUS TIB.HEMI-SPCR.T2/2+ 5MM RM/LL
04046963337902COLUMBUS TIB.HEMI-SPCR.T1/1+ 15MM RM/LL
04046963337896COLUMBUS TIB.HEMI-SPCR.T1/1+ 10MM RM/LL
04046963337858COLUMBUS TIB.HEMI-SPCR.T0/0+ 10MM RM/LL
04046963339463COLUMBUS TIB.HEMI-SPCR.T1/1+ 5MM RL/LM
04046963339432COLUMBUS TIB.HEMI-SPCR.T0/0+ 10MM RL/LM
04046963338060COLUMBUS TIB.HEMI-SPCR.T5 15MM RM/LL
04046963338053COLUMBUS TIB.HEMI-SPCR.T5 10MM RM/LL
04046963338046COLUMBUS TIB.HEMI-SPCR.T5 5MM RM/LL
04046963338015COLUMBUS TIB.HEMI-SPCR.T4/4+ 10MM RM/LL
04046963337988COLUMBUS TIB.HEMI-SPCR.T3/3+ 15MM RM/LL
04046963337971COLUMBUS TIB.HEMI-SPCR.T3/3+ 10MM RM/LL
04046963337964COLUMBUS TIB.HEMI-SPCR.T3/3+ 5MM RM/LL
04046963337940COLUMBUS TIB.HEMI-SPCR.T2/2+ 15MM RM/LL
04046963337933COLUMBUS TIB.HEMI-SPCR.T2/2+ 10MM RM/LL
04046963337889COLUMBUS TIB.HEMI-SPCR.T1/1+ 5MM RM/LL
04046963337865COLUMBUS TIB.HEMI-SPCR.T0/0+ 15MM RM/LL
04046963337841COLUMBUS TIB.HEMI-SPCR.T0/0+ 5MM RM/LL
04046963342203COLUMBUS REV FEMUR SPACER POST.F7 15MM
04046963342197COLUMBUS REV FEMUR SPACER POST.F6 15MM
04046963342180COLUMBUS REV FEMUR SPACER POST.F5 15MM
04046963342159COLUMBUS REV FEMUR SPACER POST.F7 10MM
04046963342142COLUMBUS REV FEMUR SPACER POST.F6 10MM
04046963342135COLUMBUS REV FEMUR SPACER POST.F5 10MM
04046963342128COLUMBUS REV FEMUR SPACER POST.F4 10MM
04046963342111COLUMBUS REV FEMUR SPACER POST.F3 10MM
04046963342104COLUMBUS REV FEMUR SPACER POST.F2 10MM
04046963342098COLUMBUS REV FEMUR SPACER POST.F1 10MM
04046963342074COLUMBUS REV FEMUR SPACER POST.F7 5MM
04046963342067COLUMBUS REV FEMUR SPACER POST.F6 5MM
04046963342050COLUMBUS REV FEMUR SPACER POST.F5 5MM
04046963342043COLUMBUS REV FEMUR SPACER POST.F4 5MM

Trademark Results [Columbus]

Mark Image

Registration | Serial
Company
Trademark
Application Date
COLUMBUS
COLUMBUS
98212225 not registered Live/Pending
Columbus Manufacturing, Inc.
2023-10-06
COLUMBUS
COLUMBUS
97477201 not registered Live/Pending
The Columbus Co., Ltd.
2022-06-27
COLUMBUS
COLUMBUS
90132686 not registered Live/Pending
LIBERTY COMMUNICATIONS OF PUERTO RICO LLC
2020-08-24
COLUMBUS
COLUMBUS
88464011 5943597 Live/Registered
Columbus Manufacturing, Inc.
2019-06-07
COLUMBUS
COLUMBUS
87375117 not registered Dead/Abandoned
Masco Cabinetry LLC
2017-03-17
COLUMBUS
COLUMBUS
87318710 not registered Live/Pending
Seyntex
2017-01-31
COLUMBUS
COLUMBUS
85983367 4700586 Live/Registered
Columbus Accessories
2013-04-12
COLUMBUS
COLUMBUS
85902569 not registered Dead/Abandoned
Columbus Accessories
2013-04-12
COLUMBUS
COLUMBUS
85361934 4228650 Live/Registered
COLUMBUS A/S
2011-07-01
COLUMBUS
COLUMBUS
79266257 not registered Live/Pending
RAPID MEDICAL LTD
2019-04-04
COLUMBUS
COLUMBUS
79151088 not registered Dead/Abandoned
PALUMBO GROUP S.P.A.
2014-04-01
COLUMBUS
COLUMBUS
79092363 not registered Dead/Abandoned
Collinson Group (Trademarks) Limited
2011-01-10

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