LACTOSORB* 2.0MM SYSTEM 915-2072

GUDID 00841036054274

BIOMET MICROFIXATION, INC

Bone tap, single-use, non-sterile
Primary Device ID00841036054274
NIH Device Record Key8bd74750-ebea-47f9-b453-a77a3d8b4b2f
Commercial Distribution StatusIn Commercial Distribution
Brand NameLACTOSORB* 2.0MM SYSTEM
Version Model Number915-2072
Catalog Number915-2072
Company DUNS046189866
Company NameBIOMET MICROFIXATION, INC
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 Usetrue
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(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100841036054274 [Primary]

FDA Product Code

HWXTAP, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036054274]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-15
Device Publish Date2018-09-14

On-Brand Devices [LACTOSORB* 2.0MM SYSTEM]

00841036054298915-2074
00841036054274915-2072
00841036054250915-2070
00841036054038915-2027
00841036053949915-2011
00841036053918915-2003

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