Primary Device ID | 00889024186507 |
NIH Device Record Key | 5ba43f54-90d4-4fcb-841f-f2a22d070e0d |
Commercial Distribution Discontinuation | 2017-12-18 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MG II® |
Version Model Number | 5110-75-40 |
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 | true |
Serial Number | false |
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)348-2759 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmer.com |
Length | 40 Millimeter |
Device Size Text, specify | 0 |
Length | 40 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024186507 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024186507]
Moist Heat or Steam Sterilization
[00889024186507]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MG II 74144880 1677487 Live/Registered |
ZIMMER, INC. 1991-03-06 |