Microplasty® Elite Instruments 32-484005

GUDID 00887868491542

Biomet Orthopedics, LLC

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00887868491542
NIH Device Record Key25b08055-5495-451a-a7e2-05bad7e0b96a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicroplasty® Elite Instruments
Version Model Number32-484005
Catalog Number32-484005
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868491542 [Primary]

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


[00887868491542]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-16
Device Publish Date2022-05-08

On-Brand Devices [Microplasty® Elite Instruments]

0088030445586332-485159
0088030445585632-485153
0088030445584932-485157
0088030445583232-485152
0088030445582532-485158
0088030445581832-485154
0088030445579532-485150
0088030445577132-485151
0088030445575732-484553
0088030445571932-484554
0088030445557332-485156
0088030445556632-485155
0088030445555932-484061
0088786849165832-484061
0088786849297632-484550
0088786849317132-484586
0088786849316432-484585
0088786849315732-484584
0088786849314032-484583
0088786849313332-484582
0088786849312632-484581
0088786849311932-484580
0088786849301032-484554
0088786849300332-484553
0088786849299032-484552
0088786849298332-484551
0088786849162732-484031
0088786849160332-484015
0088786849159732-484012
0088786849158032-484011
0088786849156632-484007
0088786849155932-484006
0088786849154232-484005
0088786849153532-484004
0088786849157332-484010
0088786849152832-484000
0088786849302732-484555

Trademark Results [Microplasty]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MICROPLASTY
MICROPLASTY
78218527 2846857 Live/Registered
BIOMET MANUFACTURING, LLC
2003-02-25
MICROPLASTY
MICROPLASTY
77337493 3629443 Live/Registered
Biomet Manufacturing, LLC
2007-11-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.