Primary Device ID | 00887868038686 |
NIH Device Record Key | dcc6cdfa-976a-4b4c-84ee-f587ecf0cb96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AFFIXUS®HIP FRACTURE NAIL ANTI-ROTATION SCREW |
Version Model Number | 8145-01-065 |
Catalog Number | 814501065 |
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 | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868038686 [Primary] |
HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00887868038778 | 8145-01-110 |
00887868038761 | 8145-01-105 |
00887868038754 | 8145-01-100 |
00887868038747 | 8145-01-095 |
00887868038730 | 8145-01-090 |
00887868038723 | 8145-01-085 |
00887868038716 | 8145-01-080 |
00887868038709 | 8145-01-075 |
00887868038693 | 8145-01-070 |
00887868038686 | 8145-01-065 |
00887868038679 | 8145-01-060 |
00887868038662 | 8145-01-055 |
00887868038655 | 8145-01-050 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() AFFIXUS 77944955 3912289 Live/Registered |
BIOMET C.V. 2010-02-25 |