Primary Device ID | 00887868264313 |
NIH Device Record Key | a1287a44-a1a3-47a0-84af-3ef2978fec3f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mallory-Head® Primary Hip System |
Version Model Number | 11-104112 |
Catalog Number | 11-104112 |
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 | 00887868264313 [Primary] |
LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MALLORY-HEAD 73737255 1522518 Live/Registered |
BIOMET, INC. 1988-06-29 |