A.L.P.S.MIS TARGETING GUIDE 110008305

GUDID 00887868076619

Biomet Orthopedics, LLC

Orthopaedic implant aiming/guiding block, reusable
Primary Device ID00887868076619
NIH Device Record Key7af75d41-2f80-4df9-9753-2b2de4423bdd
Commercial Distribution StatusIn Commercial Distribution
Brand NameA.L.P.S.MIS TARGETING GUIDE
Version Model Number110008305
Catalog Number110008305
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868076619 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPlate, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868076619]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-26

On-Brand Devices [A.L.P.S.MIS TARGETING GUIDE]

00887868076626110008307
00887868076619110008305
00887868076602110008303
00887868076596110008301

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