OXFORD LATERAL INSTRUMENTS 32-423352

GUDID 00880304543560

Biomet Orthopedics, LLC

Manual bone mill
Primary Device ID00880304543560
NIH Device Record Key49e8362b-79c2-4de3-9bbb-c763c2af8f42
Commercial Distribution StatusIn Commercial Distribution
Brand NameOXFORD LATERAL INSTRUMENTS
Version Model Number32-423352
Catalog Number32-423352
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 Datetrue
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 Identifiers

Device Issuing AgencyDevice ID
GS100880304543560 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304543560]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-10-05
Device Publish Date2017-07-28

On-Brand Devices [OXFORD LATERAL INSTRUMENTS]

0088030460995232-423353
0088030460994532-423350
0088030460988432-423339
0088030454356032-423352
0088030454355332-423351
0088030454354632-423341
0088030454353932-423343
0088030454352232-423344
0088030454347832-423342
0088030454344732-423340
0088030454343032-423337
0088030454342332-423338

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