DVR® Crosslock 231200006

GUDID 00880304805811

Biomet Orthopedics, LLC

Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable
Primary Device ID00880304805811
NIH Device Record Key26d30aee-dfcd-49ff-aca5-8d20a00638d5
Commercial Distribution StatusIn Commercial Distribution
Brand NameDVR® Crosslock
Version Model Number231200006
Catalog Number231200006
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 Datetrue
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
GS100880304805811 [Primary]

FDA Product Code

FSMTRAY, SURGICAL, INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


[00880304805811]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-09-16
Device Publish Date2021-09-01

On-Brand Devices [DVR® Crosslock]

00887868446351131825051
00887868446344131824051
008878684463371318-23-051
008878684463201318-22-176
008878684463131318-22-126
008878684463061318-22-091
008878684462901318-22-061
008878684462831318-22-051
008878684462761318-22-041
008878684462691318-21-051
008878684462521318-21-041
008878684462451318-20-051
00887868446238131815051
00887868446221131814051
008878684462141318-13-051
008878684462071318-12-176
008878684461911318-12-126
008878684461841318-12-091
008878684461601318-12-061
008878684461531318-12-051
008878684461461318-12-041
008878684461391318-11-051
008878684461221318-11-041
008878684461151318-10-051
00880304805811231200006

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