SSI DST AGMT PROV E 10MM

GUDID 00889024625686

Zimmer, Inc.

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Primary Device ID00889024625686
NIH Device Record Keya912420d-9660-41a2-9e92-2cec9c25c55b
Commercial Distribution Discontinuation2021-08-11
Commercial Distribution StatusNot in Commercial Distribution
Brand NameSSI DST AGMT PROV E 10MM
Version Model NumberSSI006524
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 Batchfalse
Serial Numbertrue
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

Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

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

Device Issuing AgencyDevice ID
GS100889024625686 [Primary]

FDA Product Code

HWTTemplate

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


[00889024625686]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-08-19
Device Publish Date2021-08-11

Devices Manufactured by Zimmer, Inc.

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00889024648203 - ROSA® Shoulder2024-02-29
00889024625877 - G7 25MM DRILL GUIDE2023-12-25
00889024657441 - RDCTN HNDL ASSY LRG2023-12-25
00889024658004 - PIVOTING HUMERAL EM GUIDE2023-12-25
00889024660571 - 3.5MM BALL HEX SHAFT2023-12-25
00889024661257 - REAMER ADPT PULLER2023-12-25

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