AS NB100Z

GUDID 04046964027024

AS TIBIA EXTENSION STEM D14MM L12MM

Aesculap AG

Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis Mobile-bearing total knee prosthesis
Primary Device ID04046964027024
NIH Device Record Key9e4cdcf8-9a6a-4a32-b186-9b59f848cdea
Commercial Distribution StatusIn Commercial Distribution
Brand NameAS
Version Model NumberNB100Z
Catalog NumberNB100Z
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
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104046964027024 [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 Number4
Public Version Date2020-07-01
Device Publish Date2016-11-25

On-Brand Devices [AS]

04046964027024AS TIBIA EXTENSION STEM D14MM L12MM
04046964027017AS TIBIA EXTENSION STEM D12MM L12MM
04046963124519AS TIBIAL OBTURATOR D14MM
04046963124502AS TIBIAL OBTURATOR D12MM

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