Primary Device ID | 00880304681262 |
NIH Device Record Key | 3098c7f2-dc8c-46fe-af1d-20a0dbb62061 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CEMENTON |
Version Model Number | 431291 |
Catalog Number | 431291 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304681262 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2016-09-26 |
00880304683037 | 431391 |
00880304683020 | 431387 |
00880304683013 | 431383 |
00880304683006 | 431379 |
00880304682993 | 431375 |
00880304682986 | 431371 |
00880304682979 | 431367 |
00880304682962 | 431363 |
00880304682955 | 431359 |
00880304681262 | 431291 |
00880304681255 | 431287 |
00880304681248 | 431283 |
00880304681231 | 431279 |
00880304681224 | 431275 |
00880304681217 | 431271 |
00880304681200 | 431267 |
00880304681194 | 431263 |
00880304681187 | 431259 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CEMENTON 86126664 5086968 Live/Registered |
Biomet Manufacturing, LLC 2013-11-22 |