| Primary Device ID | 00880304495432 |
| NIH Device Record Key | 3265f389-cdd3-41fd-8722-1dd9309f2711 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOMET 360 |
| Version Model Number | 32-360120 |
| Catalog Number | 32-360120 |
| 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 | false |
| 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)348-9500 |
| 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 | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304495432 [Primary] |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
Moist Heat or Steam Sterilization
[00880304495432]
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 | 2016-09-22 |
| 00880304502307 | 32-360134 |
| 00880304502239 | 32-360133 |
| 00880304502192 | 32-360132 |
| 00880304502185 | 32-360135 |
| 00880304502178 | 32-360136 |
| 00880304496149 | 32-360138 |
| 00880304495920 | 32-360137 |
| 00880304495517 | 32-360125 |
| 00880304495500 | 32-360126 |
| 00880304495456 | 32-360122 |
| 00880304495449 | 32-360128 |
| 00880304495432 | 32-360120 |
| 00880304495425 | 32-360127 |
| 00880304495340 | 32-360131 |
| 00880304495326 | 32-360121 |
| 00880304495296 | 32-360130 |
| 00880304494237 | 32-360124 |
| 00880304494183 | 32-360123 |