SA 44 MM LINER IMPACTOR SSI006718

GUDID 00889024630987

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00889024630987
NIH Device Record Key44f3d43d-ae85-4e0b-90e2-58c53144bc6f
Commercial Distribution StatusIn Commercial Distribution
Brand NameSA 44 MM LINER IMPACTOR
Version Model NumberSSI006718
Catalog NumberSSI006718
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
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 Identifiers

Device Issuing AgencyDevice ID
GS100889024630987 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


[00889024630987]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-16
Device Publish Date2022-05-06

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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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