| Primary Device ID | 00880304698185 |
| NIH Device Record Key | 28d77cb6-4379-45f5-9ee7-d84a687e1f33 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ECHO BI-METRIC |
| Version Model Number | 110025098 |
| Catalog Number | 110025098 |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304698185 [Primary] |
| OQI | Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304698185]
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 | 2017-07-28 |
| 00880304698567 | 110026867 |
| 00880304698482 | 110025764 |
| 00880304698185 | 110025098 |
| 00880304698178 | 110025102 |
| 00880304698161 | 110025101 |
| 00880304698154 | 110025093 |
| 00880304698147 | 110025090 |
| 00880304698130 | 110025099 |
| 00880304698123 | 110025095 |
| 00880304698116 | 110025094 |
| 00880304698109 | 110025087 |
| 00880304698093 | 110025097 |
| 00880304698086 | 110025091 |
| 00880304698079 | 110025092 |
| 00880304698062 | 110025089 |
| 00880304467538 | 595613 |
| 00880304467514 | 595610 |