3.5MM BALL HEX SHAFT SSI007421

GUDID 00889024660571

Zimmer, Inc.

Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00889024660571
NIH Device Record Key06a4a720-2b4b-4da1-99e2-5be974c824c4
Commercial Distribution StatusIn Commercial Distribution
Brand Name3.5MM BALL HEX SHAFT
Version Model NumberSSI007421
Catalog NumberSSI007421
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

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 Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024660571 [Primary]

FDA Product Code

HXXScrewdriver

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


[00889024660571]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-25
Device Publish Date2023-12-15

Devices Manufactured by Zimmer, Inc.

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00889024683938 - G7® Revision Acetabular System2026-02-18
00889024683945 - G7® Revision Acetabular System2026-02-18
00889024686496 - G7® Revision Acetabular System2026-02-18
00889024686502 - G7® Revision Acetabular System2026-02-18
00889024686519 - G7® Revision Acetabular System2026-02-18
00889024686526 - G7® Revision Acetabular System2026-02-18
00889024686533 - G7® Revision Acetabular System2026-02-18

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