Primary Device ID | 00887868501876 |
NIH Device Record Key | 66796095-b301-4942-b015-c9964b567444 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RingLoc®+ Hi-Wall+ |
Version Model Number | 33-108725 |
Catalog Number | 33-108725 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868501876 [Primary] |
HWT | TEMPLATE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
[00887868501876]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-16 |
Device Publish Date | 2022-05-08 |
00887868501906 | 33-108728 |
00887868501890 | 33-108727 |
00887868501883 | 33-108726 |
00887868501876 | 33-108725 |
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 |