| Primary Device ID | 00880304514331 |
| NIH Device Record Key | 4a430e87-4ebc-4aa3-836d-5a33e6a33ffa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TAPERLOC COMPLETE MICRO PRIMARY FEMORAL |
| Version Model Number | 51-106130 |
| Catalog Number | 51-106130 |
| 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 | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304514331 [Primary] |
| KWA | Prosthesis, hip, semi-constrained (metal uncemented acetabular component) |
| 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 | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00880304515314 | 51-108080 |
| 00880304515291 | 51-108070 |
| 00880304515277 | 51-108060 |
| 00880304515253 | 51-108050 |
| 00880304515239 | 51-108040 |
| 00880304514614 | 51-106090 |
| 00880304514508 | 51-106240 |
| 00880304514485 | 51-106220 |
| 00880304514461 | 51-106200 |
| 00880304514447 | 51-106180 |
| 00880304514416 | 51-106170 |
| 00880304514393 | 51-106160 |
| 00880304514379 | 51-106150 |
| 00880304514355 | 51-106140 |
| 00880304514331 | 51-106130 |
| 00880304514317 | 51-106120 |
| 00880304514294 | 51-106110 |
| 00880304514270 | 51-106100 |
| 00880304513778 | 51-107090 |
| 00880304513655 | 51-107240 |
| 00880304513631 | 51-107220 |
| 00880304513617 | 51-107200 |
| 00880304513594 | 51-107180 |
| 00880304513570 | 51-107170 |
| 00880304513556 | 51-107160 |
| 00880304513532 | 51-107150 |
| 00880304513518 | 51-107140 |
| 00880304513495 | 51-107130 |
| 00880304513471 | 51-107120 |
| 00880304513457 | 51-107110 |
| 00880304513433 | 51-107100 |
| 00880304513037 | 51-109080 |
| 00880304513013 | 51-109070 |
| 00880304512993 | 51-109060 |
| 00880304512979 | 51-109050 |