| Primary Device ID | 00887868308024 |
| NIH Device Record Key | 8f596911-d2be-4dcf-bbe3-95068eedb071 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RingLoc® Mallory-Head® Hip System |
| Version Model Number | 13-104144 |
| Catalog Number | 13-104144 |
| 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 | 00887868308024 [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 |