GUDID 00889024110939

Zimmer GmbH

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile
Primary Device ID00889024110939
NIH Device Record Key9efb3b57-5203-4534-ae36-4bed7360f77f
Commercial Distribution StatusIn Commercial Distribution
Version Model Number35.18.026
Company DUNS488133448
Company NameZimmer GmbH
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
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@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com

Device Dimensions

Length26 Millimeter
Outer Diameter1.8 Millimeter
Device Size Text, specify0
Length26 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024110939 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTNWASHER, BOLT NUT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024110939]

Moist Heat or Steam Sterilization


[00889024110939]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-12-30

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