DRILL POINT K-WIRE 909827

GUDID 00880304412804

Biomet Orthopedics, LLC

Bone nail guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable
Primary Device ID00880304412804
NIH Device Record Key3895d8b4-e32b-4748-9eee-8b2186d1c62b
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRILL POINT K-WIRE
Version Model Number909827
Catalog Number909827
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 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 Identifiers

Device Issuing AgencyDevice ID
GS100880304412804 [Primary]

FDA Product Code

HWBEXTRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


[00880304412804]

Moist Heat or Steam Sterilization


Device Entry Metadata

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

On-Brand Devices [DRILL POINT K-WIRE]

00880304412804909827
00880304412842909832

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