AS ENDURO NB057Z

GUDID 04046963177904

AS ENDURO TIBIA HEMI-WEDGE T2 12MM 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
Primary Device ID04046963177904
NIH Device Record Key686d211c-b0a7-4b23-91ab-1feefb05a014
Commercial Distribution StatusIn Commercial Distribution
Brand NameAS ENDURO
Version Model NumberNB057Z
Catalog NumberNB057Z
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104046963177904 [Primary]

FDA Product Code

KROPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-04-02
Device Publish Date2015-09-24

On-Brand Devices [AS ENDURO]

04046963177935AS ENDURO TIBIA HEMI-WEDGE T3 16MM RL/LM
04046963177928AS ENDURO TIBIA HEMI-WEDGE T2 16MM RL/LM
04046963177911AS ENDURO TIBIA HEMI-WEDGE T3 12MM RL/LM
04046963177904AS ENDURO TIBIA HEMI-WEDGE T2 12MM RL/LM
04046963177881AS ENDURO TIBIA HEMI-WEDGE T3 8MM RL/LM
04046963177867AS ENDURO TIBIA HEMI-WEDGE T2 8MM RL/LM
04046963177850AS ENDURO TIBIA HEMI-WEDGE T3 4MM RL/LM
04046963177836AS ENDURO TIBIA HEMI-WEDGE T2 4MM RL/LM
04046963177812AS ENDURO TIBIA HEMI-WEDGE T3 16MM RM/LL
04046963177805AS ENDURO TIBIA HEMI-WEDGE T2 16MM RM/LL
04046963177799AS ENDURO TIBIA HEMI-WEDGE T3 12MM RM/LL
04046963177775AS ENDURO TIBIA HEMI-WEDGE T2 12MM RM/LL
04046963177751AS ENDURO TIBIA HEMI-WEDGE T3 8MM RM/LL
04046963177744AS ENDURO TIBIA HEMI-WEDGE T2 8MM RM/LL
04046963177737AS ENDURO TIBIA HEMI-WEDGE T3 4MM RM/LL
04046963177713AS ENDURO TIBIA HEMI-WEDGE T2 4MM RM/LL
04046963177706AS ENDURO TIBIA HEMI-WEDGE T1 16MM RL/LM
04046963177683AS ENDURO TIBIA HEMI-WEDGE T1 12MM RL/LM
04046963177676AS ENDURO TIBIA HEMI-WEDGE T1 8MM RL/LM
04046963177621AS ENDURO TIBIA HEMI-WEDGE T1 4MM RL/LM
04046963177591AS ENDURO TIBIA HEMI-WEDGE T1 16MM RM/LL
04046963177584AS ENDURO TIBIA HEMI-WEDGE T1 12MM RM/LL
04046963177577AS ENDURO TIBIA HEMI-WEDGE T1 8MM RM/LL
04046963177560AS ENDURO TIBIA HEMI-WEDGE T1 4MM RM/LL

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