Solid Hexalobular Driver AO 110009961

GUDID 00887868522772

Biomet Orthopedics, LLC

Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver
Primary Device ID00887868522772
NIH Device Record Key2ee3ab8b-a342-4a22-9339-788ea8f1ebba
Commercial Distribution StatusIn Commercial Distribution
Brand NameSolid Hexalobular Driver AO
Version Model Number110009961
Catalog Number110009961
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
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
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
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868522772 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

Moist Heat or Steam Sterilization


[00887868522772]

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 AO]

00887868111419110009965
00887868111402110009963
00887868111396110009961
00887868522796110009965
00887868522789110009963
00887868522772110009961

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