Nexel®

GUDID 00889024274327

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use Orthopaedic prosthesis implantation positioning instrument, single-use
Primary Device ID00889024274327
NIH Device Record Key27aef301-c761-48e4-9ca3-e0b9c58c3815
Commercial Distribution StatusIn Commercial Distribution
Brand NameNexel®
Version Model Number47-8401-038-00
Company DUNS056038268
Company NameZimmer, Inc.
Device Count2
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(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024274327 [Primary]
GS100889024466296 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDCPROSTHESIS, ELBOW, CONSTRAINED, CEMENTED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-07
Device Publish Date2016-08-09

On-Brand Devices [Nexel®]

0088902427432747-8401-038-00
0088902427220000-8401-080-00
0088902427152400-8401-000-32
0088902427151700-8401-000-31
0088902427150000-8401-000-22
0088902427149400-8401-000-21
0088902427148700-8401-000-12
0088902427147000-8401-000-11
0088902446629647-8401-038-00

Trademark Results [Nexel]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NEXEL
NEXEL
90254764 not registered Live/Pending
Nexel Technologies Corporation
2020-10-14
NEXEL
NEXEL
90141339 not registered Live/Pending
NEXEL TECHNOLOGIES CORPORATION
2020-08-27
NEXEL
NEXEL
88024092 not registered Live/Pending
Kingsberg, George
2018-07-03
NEXEL
NEXEL
87979048 5634674 Live/Registered
Nexel Industries, Inc.
2016-11-03
NEXEL
NEXEL
87975692 5293001 Live/Registered
Nexel Industries, Inc.
2016-11-03
NEXEL
NEXEL
87709026 5513060 Live/Registered
Nexel Industries, Inc.
2017-12-05
NEXEL
NEXEL
87495635 5419950 Live/Registered
Nexel Industries, Inc.
2017-06-19
NEXEL
NEXEL
87225437 not registered Live/Pending
Nexel Industries, Inc.
2016-11-03
NEXEL
NEXEL
86887318 5031814 Live/Registered
Nexel Industries, Inc.
2016-01-26
NEXEL
NEXEL
85730768 4433700 Live/Registered
Zimmer, Inc.
2012-09-17
NEXEL
NEXEL
74493288 not registered Dead/Abandoned
Accelerated Systems, Inc.
1994-02-22
NEXEL
NEXEL
74059539 1717888 Live/Registered
Global Equipment Company
1990-05-16

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