Primary Device ID | 00880304517196 |
NIH Device Record Key | 4fbe8569-a1a2-4094-8dd4-520843d136ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TAPERLOC COMPLETE XR 123 FEMORAL |
Version Model Number | 51-105180 |
Catalog Number | 51-105180 |
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 | 00880304517196 [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 |
00880304517196 | 51-105180 |
00880304517189 | 51-105170 |
00880304517172 | 51-105160 |
00880304517165 | 51-105150 |
00880304517158 | 51-105140 |
00880304517141 | 51-105130 |
00880304517134 | 51-105120 |
00880304517127 | 51-105110 |
00880304517110 | 51-105100 |
00880304517103 | 51-105090 |
00880304516915 | 51-102080 |
00880304516908 | 51-102070 |
00880304516892 | 51-102060 |
00880304516885 | 51-102050 |
00880304516878 | 51-102040 |
00880304517226 | 51-105240 |
00880304517219 | 51-105220 |
00880304517202 | 51-105200 |