Primary Device ID | 00880304521063 |
NIH Device Record Key | a6b2a65c-baff-4b1f-9c5e-93d351c5ffe4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STAGEONE SELECT |
Version Model Number | 431185 |
Catalog Number | 431185 |
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 | true |
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 |
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 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 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 | 00880304521063 [Primary] |
KWL | Prosthesis, hip, hemi-, femoral, metal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2015-10-24 |
00880304521995 | 431190 |
00880304521254 | 431183 |
00880304521247 | 431192 |
00880304521230 | 431191 |
00880304521179 | 431193 |
00880304521162 | 431199 |
00880304521155 | 431194 |
00880304521148 | 431197 |
00880304521131 | 431198 |
00880304521124 | 431195 |
00880304521117 | 431196 |
00880304521100 | 431181 |
00880304521094 | 431188 |
00880304521087 | 431186 |
00880304521070 | 431187 |
00880304521063 | 431185 |
00880304521056 | 431184 |
00880304521032 | 431182 |