Primary Device ID | 00880304228344 |
NIH Device Record Key | 172a71ae-37fb-4a6f-bdb0-107ea028da2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BIO-MOORE ENDO II HIP SYSTEM |
Version Model Number | 139246 |
Catalog Number | 139246 |
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 | 00880304228344 [Primary] |
JDG | Prosthesis, hip, femoral component, cemented, metal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00880304228382 | 139249 |
00880304228375 | 139248 |
00880304228351 | 139247 |
00880304228344 | 139246 |
00880304228337 | 139245 |
00880304221918 | 12-139044 |
00880304221901 | 12-139042 |
00880304221895 | 12-139038 |
00880304221888 | 12-139036 |
00880304221871 | 12-139034 |
00880304221857 | 12-139032 |
00880304221840 | 12-139030 |
00880304221833 | 12-139028 |
00880304221826 | 12-139026 |
00880304221819 | 12-139024 |
00880304221802 | 12-139022 |
00880304221772 | 12-139018 |
00880304221758 | 12-139016 |
00880304221734 | 12-139014 |
00880304221727 | 12-139012 |
00880304221710 | 12-139010 |
00880304221703 | 12-139008 |
00880304221697 | 12-139006 |
00880304007499 | 12-139046 |
00880304001565 | 12-139040 |
00880304221789 | 12-139020 |