Primary Device ID | 00888480237310 |
NIH Device Record Key | 3d3af566-384e-4b8e-91b3-9d240d166838 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PEANUT PLATING SYSTEM |
Version Model Number | 24724 |
Catalog Number | 24724 |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888480237310 [Primary] |
HWC | Screw, fixation, bone |
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 |
00880304532373 | 24516 |
00880304500433 | 24616 |
00880304500426 | 24612 |
00880304500419 | 24632 |
00880304500402 | 24540 |
00880304492530 | 24524 |
00880304491571 | 24636 |
00880304491526 | 24532 |
00888480237334 | 24740 |
00888480237327 | 24732 |
00888480237310 | 24724 |
00888480237303 | 24716 |