Primary Device ID | 00887868037924 |
NIH Device Record Key | ea8e5684-cdc0-489f-aa77-a70398d1605f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PEAK FX™LC CAP |
Version Model Number | 8142-35-105 |
Catalog Number | 814235105 |
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 | 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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868037924 [Primary] |
KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868037924]
Moist Heat or Steam Sterilization
[00887868037924]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00887868037948 | 8142-35-120 |
00887868037931 | 8142-35-115 |
00887868037924 | 8142-35-105 |
00887868037917 | 8142-35-100 |
00887868037900 | 8142-35-020 |
00887868037894 | 8142-35-015 |
00887868037887 | 8142-35-010 |
00887868037870 | 8142-35-005 |
00887868037863 | 8142-35-000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PEAK FX 78867976 not registered Dead/Abandoned |
DePuy, Inc. 2006-04-24 |
PEAK FX 75923271 2587226 Dead/Cancelled |
Neways, Inc. 2000-02-18 |