AS Columbus® REVISION NR254Z

GUDID 04046963989071

AS COLUMBUS TIB.HEMI-SP.T3/3+ 15MM 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
Primary Device ID04046963989071
NIH Device Record Key251ceed8-915c-49d0-ba8a-dc9bc48c5a35
Commercial Distribution StatusIn Commercial Distribution
Brand NameAS Columbus® REVISION
Version Model NumberNR254Z
Catalog NumberNR254Z
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]
GS104046963989071 [Primary]

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
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 [AS Columbus® REVISION]

04046963989095AS COLUMBUS TIB.HEMI-SP.T5 15MM RL/LM
04046963989088AS COLUMBUS TIB.HEMI-SP.T4/4+ 15MM RL/LM
04046963989071AS COLUMBUS TIB.HEMI-SP.T3/3+ 15MM RL/LM
04046963989064AS COLUMBUS TIB.HEMI-SP.T2/2+ 15MM RL/LM
04046963989057AS COLUMBUS TIB.HEMI-SP.T1/1+ 15MM RL/LM
04046963989040AS COLUMBUS TIB.HEMI-SP.T0/0+ 15MM RL/LM
04046963988920AS COLUMBUS TIB.HEMI-SP.T5 15MM RM/LL
04046963988654AS COLUMBUS TIB.HEMI-SP.T3/3+ 15MM RM/LL
04046963988647AS COLUMBUS TIB.HEMI-SP.T2/2+ 15MM RM/LL
04046963988630AS COLUMBUS TIB.HEMI-SP.T1/1+ 15MM RM/LL
04046963177126AS COLUMBUS TIB.HEMI-SP.T5 10MM RL/LM
04046963177119AS COLUMBUS TIB.HEMI-SP.T4/4+ 10MM RL/LM
04046963177102AS COLUMBUS TIB.HEMI-SP.T3/3+ 10MM RL/LM
04046963177096AS COLUMBUS TIB.HEMI-SP.T2/2+ 10MM RL/LM
04046963177089AS COLUMBUS TIB.HEMI-SP.T1/1+ 10MM RL/LM
04046963177065AS COLUMBUS TIB.HEMI-SP.T5 5MM RL/LM
04046963177058AS COLUMBUS TIB.HEMI-SP.T4/4+ 5MM RL/LM
04046963177041AS COLUMBUS TIB.HEMI-SP.T3/3+ 5MM RL/LM
04046963177034AS COLUMBUS TIB.HEMI-SP.T2/2+ 5MM RL/LM
04046963176969AS COLUMBUS TIB.HEMI-SP.T2/2+ 10MM RM/LL
04046963176952AS COLUMBUS TIB.HEMI-SP.T1/1+ 10MM RM/LL
04046963176938AS COLUMBUS TIB.HEMI-SP.T5 5MM RM/LL
04046963176891AS COLUMBUS TIB.HEMI-SP.T1/1+ 5MM RM/LL

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