00-0471-001-00

GUDID 00889024023215

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable
Primary Device ID00889024023215
NIH Device Record Key680a19b2-dbeb-4ffd-b962-12dfb2c3e4c5
Commercial Distribution StatusIn Commercial Distribution
Version Model Number471-01
Catalog Number00-0471-001-00
Company DUNS056038268
Company NameZimmer, Inc.
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 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)348-2759
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 Dimensions

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 Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024023215 [Primary]

FDA Product Code

HWLSET, HOLLOW MILL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


[00889024023215]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-08-12
Device Publish Date2016-07-26

Devices Manufactured by Zimmer, Inc.

00889024678736 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678743 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678750 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678767 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678774 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678781 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678798 - OsseoFit™ Stemless Shoulder2024-12-26
00889024678804 - OsseoFit™ Stemless Shoulder2024-12-26

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