Primary Device ID | 00880304006966 |
NIH Device Record Key | f4f06aa9-fd50-4cc1-8224-a24ae3d58493 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BI-ANGULAR SYSTEM |
Version Model Number | 114053 |
Catalog Number | 114053 |
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 | 00880304006966 [Primary] |
MBF | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, 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 |
00880304215122 | 114094 |
00880304215016 | 114063 |
00880304214996 | 114061 |
00880304214903 | 114052 |
00880304214897 | 114029 |
00880304214880 | 114028 |
00880304214873 | 114027 |
00880304214866 | 114026 |
00880304214859 | 114025 |
00880304214842 | 114023 |
00880304009622 | 114022 |
00880304007055 | 114054 |
00880304006966 | 114053 |
00880304003927 | 114090 |
00880304003910 | 114092 |
00880304003453 | 114073 |
00880304002531 | 114024 |
00880304001329 | 114071 |
00880304001275 | 114072 |