Solid Hexalobular Driver ZH 110009967

GUDID 00887868522802

Biomet Orthopedics, LLC

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Primary Device ID00887868522802
NIH Device Record Key09be5f4b-aba3-4fa4-9f4d-a5cca4618138
Commercial Distribution StatusIn Commercial Distribution
Brand NameSolid Hexalobular Driver ZH
Version Model Number110009967
Catalog Number110009967
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
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
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Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868522802 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


[00887868522802]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-28
Device Publish Date2020-12-19

On-Brand Devices [Solid Hexalobular Driver ZH]

00887868111426110009967
00887868522802110009967

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