ZMS®

GUDID 00889024085008

Zimmer, Inc.

Orthopaedic bone wire
Primary Device ID00889024085008
NIH Device Record Key6c25a1e2-81d6-4d05-bad1-24da4b2714e9
Commercial Distribution StatusIn Commercial Distribution
Brand NameZMS®
Version Model Number47-2237-33
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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

Device Size Text, specify0
Length100 Centimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024085008 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-02-09

On-Brand Devices [ZMS®]

0088902458181447-2237-37
0088902458180747-2237-33
0088902458182147-2237-38
0088902408501547-2237-37
0088902408500847-2237-33
008890240413492246-62
008890240413252246-23
008890240400522239-01
008890240398582237-55
008890240398412237-54
008890240398342237-53
008890240398102237-46
008890240397732237-37
008890240397662237-33
008890240397592237-08
008890240397422237-05

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