Primary Device ID | 00887868308109 |
NIH Device Record Key | eda687d7-fcae-4664-8413-4354c3dd1514 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RingLoc® Mallory-Head® Hip System |
Version Model Number | 13-104160 |
Catalog Number | 13-104160 |
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 | 00887868308109 [Primary] |
MEH | Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-26 |
Device Publish Date | 2019-04-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RINGLOC 75014549 not registered Dead/Abandoned |
Aesculap AG 1995-11-03 |
RINGLOC 74307357 1811999 Live/Registered |
Biomet Manufacturing, LLC 1992-08-24 |