AS Columbus® NN596Z

GUDID 04046963367725

AS COLUMBUS TIB.HEMI-SP.T5 8MM 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 ID04046963367725
NIH Device Record Keyeecd54a4-8090-4df2-be78-48fc2d612f22
Commercial Distribution StatusIn Commercial Distribution
Brand NameAS Columbus®
Version Model NumberNN596Z
Catalog NumberNN596Z
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [Primary]
GS104046963367725 [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®]

04046963367527AS COLUMBUS TIB.HEMI-SP.T4/4+ 4MM RM/LL
04046963367497AS COLUMBUS TIB.HEMI-SP.T1/1+ 4MM RM/LL
04046963367725AS COLUMBUS TIB.HEMI-SP.T5 8MM RL/LM
04046963367718AS COLUMBUS TIB.HEMI-SP.T4/4+ 8MM RL/LM
04046963367701AS COLUMBUS TIB.HEMI-SP.T3/3+ 8MM RL/LM
04046963367695AS COLUMBUS TIB.HEMI-SP.T2/2+ 8MM RL/LM
04046963367657AS COLUMBUS TIB.HEMI-SP.T4/4+ 4MM RL/LM
04046963367640AS COLUMBUS TIB.HEMI-SP.T3/3+ 4MM RL/LM
04046963367633AS COLUMBUS TIB.HEMI-SP.T2/2+ 4MM RL/LM
04046963367572AS COLUMBUS TIB.HEMI-SP.T3/3+ 8MM RM/LL
04046963367510AS COLUMBUS TIB.HEMI-SP.T3/3+ 4MM RM/LL

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