MAXIM KNEE INSTRUMENTATION RD140512

GUDID 05019279031900

Biomet Uk Ltd

Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable Osteotomy guide, reusable
Primary Device ID05019279031900
NIH Device Record Key8c1457dc-6694-4905-bc45-f04c151c9325
Commercial Distribution StatusIn Commercial Distribution
Brand NameMAXIM KNEE INSTRUMENTATION
Version Model NumberRD140512
Catalog NumberRD140512
Company DUNS219322575
Company NameBiomet Uk Ltd
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

Device Identifiers

Device Issuing AgencyDevice ID
GS105019279031900 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


[05019279031900]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-09-22
Device Publish Date2020-05-23

On-Brand Devices [MAXIM KNEE INSTRUMENTATION]

0501927979647232-379660
05019279031917RD140513
05019279031900RD140512
0501927946726632-348086
0501927946688732-348054
0501927946597232-347127

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