K-Wire Depth Gauge 110018535

GUDID 00887868467240

Biomet Orthopedics, LLC

Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable
Primary Device ID00887868467240
NIH Device Record Keyefb60810-98c4-4cfa-975b-50986c6e5843
Commercial Distribution StatusIn Commercial Distribution
Brand NameK-Wire Depth Gauge
Version Model Number110018535
Catalog Number110018535
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

Device Dimensions

Device Size Text, specify0
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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 Identifiers

Device Issuing AgencyDevice ID
GS100887868467240 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


[00887868467240]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-04-12
Device Publish Date2021-04-02

On-Brand Devices [K-Wire Depth Gauge]

008878680244672141-40-000
0088786800227414232
0088786800171013545
008878680494228241-98-000
0088786845823113545
00887868467240110018535

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