Primary Device ID | 00880304010321 |
NIH Device Record Key | 40f3f9de-7d26-4c4a-8dc1-9b6ae340a921 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INTEGRAL 180 HIP SYSTEM |
Version Model Number | 166013 |
Catalog Number | 166013 |
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 | 00880304010321 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
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 |
00880304257870 | 166019 |
00880304257863 | 166018 |
00880304257856 | 166016 |
00880304257849 | 166015 |
00880304257832 | 166014 |
00880304257801 | 166012 |
00880304257788 | 166010 |
00880304210066 | 11-166019 |
00880304210059 | 11-166018 |
00880304210042 | 11-166017 |
00880304210035 | 11-166016 |
00880304210011 | 11-166015 |
00880304210004 | 11-166014 |
00880304209992 | 11-166013 |
00880304209985 | 11-166012 |
00880304209978 | 11-166011 |
00880304010321 | 166013 |
00880304010307 | 166017 |
00880304010291 | 166011 |