Primary Device ID | 00880304268616 |
NIH Device Record Key | 0ffcb305-0908-4010-9035-59525e860638 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BALANCE HIP SYSTEM |
Version Model Number | 180011 |
Catalog Number | 180011 |
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 | 00880304268616 [Primary] |
KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or 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 | 2019-05-22 |
Device Publish Date | 2015-10-24 |
00880304268739 | 180023 |
00880304268722 | 180022 |
00880304268715 | 180021 |
00880304268708 | 180020 |
00880304268692 | 180019 |
00880304268685 | 180018 |
00880304268678 | 180017 |
00880304268661 | 180016 |
00880304268654 | 180015 |
00880304268647 | 180014 |
00880304268630 | 180013 |
00880304268623 | 180012 |
00880304268616 | 180011 |
00880304268609 | 180010 |
00880304268593 | 180009 |
00880304268586 | 180008 |
00880304268579 | 180007 |
00880304268562 | 180006 |
00880304268555 | 180005 |
00880304268548 | 180004 |
00880304268531 | 180003 |
00880304268524 | 180002 |
00880304268517 | 180001 |
00880304268500 | 180000 |
00880304258761 | 170099 |
00880304258754 | 170098 |
00880304258747 | 170097 |
00880304258730 | 170096 |