Primary Device ID | 00880304253599 |
NIH Device Record Key | 8c046d20-caad-4e63-8d0b-55095aecfa80 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GENERATION 4 HIP SYSTEM |
Version Model Number | 162787 |
Catalog Number | 162787 |
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 | 00880304253599 [Primary] |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
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 |
00880304591332 | 11-165017 |
00880304591325 | 11-165015 |
00880304591318 | 11-165013 |
00880304591301 | 11-165011 |
00880304591295 | 11-165009 |
00880304554764 | 165017 |
00880304554757 | 165015 |
00880304521858 | 165013 |
00880304497405 | 165009 |
00880304457577 | 165011 |
00880304253599 | 162787 |
00880304253582 | 162786 |
00880304253568 | 162784 |
00880304253544 | 162782 |
00880304253537 | 162781 |