Primary Device ID | 00880304698116 |
NIH Device Record Key | 1754c316-4997-494f-9c55-e2064fe51fa9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ECHO BI-METRIC |
Version Model Number | 110025094 |
Catalog Number | 110025094 |
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 | 00880304698116 [Primary] |
OQH | Hip, semi-constrained, cemented, metal/polymer + additive, cemented |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304698116]
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 |