Primary Device ID | 00880304057395 |
NIH Device Record Key | 1f60045b-0838-41b5-ac47-fdb9da873f00 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROGRESSIVE HIP SYSTEM |
Version Model Number | CP156640 |
Catalog Number | CP156640 |
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 | 00880304057395 [Primary] |
LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-30 |
Device Publish Date | 2015-10-24 |
00880304258273 | 166331 |
00880304258266 | 166330 |
00880304258259 | 166329 |
00880304258242 | 166328 |
00880304258235 | 166327 |
00880304258228 | 166326 |
00880304258211 | 166325 |
00880304258204 | 166324 |
00880304258181 | 166323 |
00880304258174 | 166322 |
00880304258167 | 166321 |
00880304258150 | 166320 |
00880304258143 | 166319 |
00880304258136 | 166318 |
00880304258129 | 166317 |
00880304258112 | 166316 |
00880304258105 | 166315 |
00880304258082 | 166314 |
00880304057418 | CP156642 |
00880304057401 | CP156641 |
00880304057395 | CP156640 |
00880304057340 | CP156526 |
00880304057333 | CP156525 |
00880304057326 | CP156524 |
00880304057319 | CP156523 |
00880304057302 | CP156522 |