Ardis®

GUDID 00889024333628

ZIMMER SPINE, INC.

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage
Primary Device ID00889024333628
NIH Device Record Key21ef7cc9-cbca-4d25-9a10-fac426dd62f7
Commercial Distribution StatusIn Commercial Distribution
Brand NameArdis®
Version Model Number3201-090930
Company DUNS787663400
Company NameZIMMER SPINE, INC.
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 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(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com
Phone+1(866)774-6368
Emailzimmer.consumerrelations@zimmer.com

Device Dimensions

Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter
Height9 Millimeter
Length30 Millimeter
Width9 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024333628 [Primary]

FDA Product Code

MAXIntervertebral fusion device with bone graft, lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-02-24
Device Publish Date2016-07-21

On-Brand Devices [Ardis®]

008890243348543260-01
008890243348473258-02
008890243348303258-01
008890243340763201-161134
008890243340693201-161130
008890243340523201-161126
008890243340453201-160930
008890243340383201-160926
008890243340213201-160922
008890243340143201-151134
008890243340073201-151130
008890243339943201-151126
008890243339873201-150930
008890243339703201-150926
008890243339633201-150922
008890243339563201-141134
008890243339493201-141130
008890243339323201-141126
008890243339253201-140930
008890243339183201-140926
008890243339013201-140922
008890243338953201-131134
008890243338883201-131130
008890243338713201-131126
008890243338643201-130930
008890243338573201-130926
008890243338403201-130922
008890243338333201-121134
008890243338263201-121130
008890243338193201-121126
008890243338023201-120930
008890243337963201-120926
008890243337893201-120922
008890243337723201-111134
008890243337653201-111130
008890243337583201-111126
008890243337413201-110930
008890243337343201-110926
008890243337273201-110922
008890243337103201-101134
008890243337033201-101130
008890243336973201-101126
008890243336803201-100930
008890243336733201-100926
008890243336663201-100922
008890243336593201-091134
008890243336423201-091130
008890243336353201-091126
008890243336283201-090930
008890243336113201-090926

Trademark Results [Ardis]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ARDIS
ARDIS
97806326 not registered Live/Pending
Ardis Dispute Resolution, P.B.C.
2023-02-22
ARDIS
ARDIS
97702088 not registered Live/Pending
KBR Wyle Services, LLC
2022-12-02
ARDIS
ARDIS
90083919 not registered Live/Pending
Ardis Welness, LLC
2020-07-30
ARDIS
ARDIS
88316384 not registered Live/Pending
Ardis Wellness, LLC
2019-02-26
ARDIS
ARDIS
79272389 not registered Live/Pending
ARDIS INFORMATION SYSTEMS NV
2019-09-16
ARDIS
ARDIS
79002655 3029285 Dead/Cancelled
Eberhard-Karls-Universität Tübingen Universitätsklinikum
2003-12-22
ARDIS
ARDIS
77293169 3535083 Live/Registered
ZIMMER BIOMET SPINE, INC.
2007-10-01
ARDIS
ARDIS
74048822 1653230 Dead/Cancelled
ARDIS Company
1990-04-12
ARDIS
ARDIS
74048821 1651720 Dead/Cancelled
ARDIS COMPANY
1990-04-12
ARDIS
ARDIS
74048820 1877124 Dead/Cancelled
ARDIS Company
1990-04-12
ARDIS
ARDIS
74048819 1647678 Dead/Cancelled
ARDIS Company
1990-04-12
ARDIS
ARDIS
74048818 1649711 Dead/Cancelled
ARDIS COMPANY
1990-04-12
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