Primary Device ID | 00889024058064 |
NIH Device Record Key | b2d9e818-763f-4c8b-ab6f-3e10d9168f15 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 2359-30-18 |
Catalog Number | 00-2359-030-18 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
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 | 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)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024058064 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024058064]
Moist Heat or Steam Sterilization
[00889024058064]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-17 |
Device Publish Date | 2016-06-30 |
00889024660595 - BIOMET Anterior Adapter | 2024-04-23 |
00889024660601 - BIOMET Posterior Adapter | 2024-04-23 |
00889024660816 - +9MM Spacer Block C/D 10mm | 2024-04-23 |
00889024660823 - +9MM Spacer Block C/D 12mm | 2024-04-23 |
00889024660830 - +9MM Spacer Block C/D 14mm | 2024-04-23 |
00889024660847 - +9MM Spacer Block C/D 16mm | 2024-04-23 |
00889024660854 - +9MM Spacer Block C/D 18mm | 2024-04-23 |
00889024660861 - +9MM Spacer Block C/D 20mm | 2024-04-23 |