TM Slot Guide SSI005885

GUDID 00889024588929

Zimmer, Inc.

Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable
Primary Device ID00889024588929
NIH Device Record Key45add7e9-8ae9-4450-8513-996c126a0abd
Commercial Distribution StatusIn Commercial Distribution
Brand NameTM Slot Guide
Version Model NumberSSI005885
Catalog NumberSSI005885
Company DUNS056038268
Company NameZimmer, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

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 Identifiers

Device Issuing AgencyDevice ID
GS100889024588929 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


[00889024588929]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-10-19
Device Publish Date2020-06-08

On-Brand Devices [TM Slot Guide]

00889024588929SSI005885
00889024588912SSI005884
00889024588905SSI005883

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.