Primary Device ID | 00889024585331 |
NIH Device Record Key | 57cb19d1-540d-4fe5-9c70-4ded3914de9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MODIFIED MINI TRAY STD 3MM OFFSET |
Version Model Number | SSI005787 |
Catalog Number | SSI005787 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 |
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 | 00889024585331 [Primary] |
PAO | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-21 |
Device Publish Date | 2020-01-13 |
00887868254451 - Comprehensive® Reverse Shoulder | 2024-11-21 |
00887868578250 - Comprehensive® | 2024-11-13 |
08428898885684 - BIPASS DISPOSABLE PUSHER | 2024-09-11 |
08428898885691 - BIPASS DISPOSABLE PUSHER | 2024-09-11 |
00880304338548 - AGC ANTERIOR FILE | 2024-09-11 |
00880304339224 - PARALLEL PULLER | 2024-09-11 |
00880304342187 - AGC MODULAR TIBIAL II | 2024-09-11 |
00880304365247 - BIO-MODULAR | 2024-09-11 |