Primary Device ID | 00880304514461 |
NIH Device Record Key | 4cdd0a2d-00ad-4d16-b7bc-b1c64f2b45d4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TAPERLOC COMPLETE MICRO PRIMARY FEMORAL |
Version Model Number | 51-106200 |
Catalog Number | 51-106200 |
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 |
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 | 00880304514461 [Primary] |
OQG | Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, 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 |
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 |