COMPREHENSIVE INSTRUMENTATION 405889

GUDID 00880304469877

Biomet Orthopedics, LLC

Fluted surgical drill bit, single-use, sterile
Primary Device ID00880304469877
NIH Device Record Keye4c96eb6-e64c-475c-8e2f-546a8b2c5e20
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOMPREHENSIVE INSTRUMENTATION
Version Model Number405889
Catalog Number405889
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
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
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
GS100880304469877 [Primary]

FDA Product Code

HTWBIT, DRILL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-11-22
Device Publish Date2017-07-28

On-Brand Devices [COMPREHENSIVE INSTRUMENTATION]

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00880304731523110029136
00880304731509110028880
00880304731394110028879
00880304731387110028878
00880304731332110028439
00880304731325110028438
00880304716209110016888
00880304716193110016887
00880304716186110016886
00880304716179110016885
00880304716162110016884
00880304716155110016883
00880304702769110017268
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00880304472785405988
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00880304471191405806
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00880304470385405970
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00880304470255405998
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00880304470002405955
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00880304469983405995
00880304469976405890
00880304469914405887
00880304469907405832
00880304469891405808
00880304469884405895
00880304469877405889
00880304469860405883
00880304469853405908
00880304469846405899
00880304469815405813
00880304469808405940
00880304469792405816
00880304469785405826
00880304469778405906
00880304469761405810
00880304469754405823
00880304469747405902
00880304469730405820
00880304469716405802

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