Primary Device ID | 00880304517301 |
NIH Device Record Key | fb399c3d-2682-4d5e-bc14-12ee8c82ce1e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TAPERLOC COMPLETE XR 123 MICRO FEMORAL |
Version Model Number | 51-145110 |
Catalog Number | 51-145110 |
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 | 00880304517301 [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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00880304517455 | 51-149080 |
00880304517448 | 51-149070 |
00880304517431 | 51-149060 |
00880304517424 | 51-149050 |
00880304517417 | 51-149040 |
00880304517370 | 51-145180 |
00880304517363 | 51-145170 |
00880304517356 | 51-145160 |
00880304517349 | 51-145150 |
00880304517332 | 51-145140 |
00880304517325 | 51-145130 |
00880304517318 | 51-145120 |
00880304517301 | 51-145110 |
00880304517295 | 51-145100 |
00880304517288 | 51-145090 |