Primary Device ID | 00889024478664 |
NIH Device Record Key | 7b360fb1-6880-4d4c-b86e-b5dd1375cc9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NexGen LCCK Knee System |
Version Model Number | 82-0156-869-11 |
Catalog Number | 82-0156-869-11 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | 1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Height | 10 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024478664 [Primary] |
JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
[00889024478664]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-11-14 |
00889024478664 | 82-0156-869-11 |
00889024478657 | 82-0156-869-10 |
00889024478640 | 82-0156-869-09 |
00889024478633 | 82-0156-869-08 |
00889024478626 | 82-0156-869-07 |
00889024478619 | 82-0156-869-06 |
00889024478602 | 82-0156-869-05 |
00889024478596 | 82-0156-869-04 |
00889024478589 | 82-0156-869-03 |
00889024478572 | 82-0156-869-02 |
00889024478565 | 82-0156-869-01 |
00889024478558 | 82-0156-869-00 |