E-XPE Patellar, on set, 3 pegs 2403-5240

GUDID 04719872149910

E-XPE Patellar, on set, 3 pegs, large, Ø35 mm

UNITED ORTHOPEDIC CORP.

Posterior-stabilized total knee prosthesis
Primary Device ID04719872149910
NIH Device Record Key44dde9fb-ebf1-43d3-8df0-3a03d9eeaaa9
Commercial Distribution StatusIn Commercial Distribution
Brand NameE-XPE Patellar, on set, 3 pegs
Version Model Number2403-5240
Catalog Number2403-5240
Company DUNS656700556
Company NameUNITED ORTHOPEDIC CORP.
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 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+886229294567
Emailservice@uoc.com.tw

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104719872149910 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-31
Device Publish Date2017-03-24

On-Brand Devices [E-XPE Patellar, on set, 3 pegs]

04719872149941E-XPE Patellar, on set, 3 pegs, E-large, Ø44 mm
04719872149934E-XPE Patellar, on set, 3 pegs, XX-large, Ø41 mm
04719872149927E-XPE Patellar, on set, 3 pegs, X-large, Ø38 mm
04719872149910E-XPE Patellar, on set, 3 pegs, large, Ø35 mm
04719872149903E-XPE Patellar, on set, 3 pegs, medium,Ø32 mm
04719872149897E-XPE Patellar, on set, 3 pegs, small, Ø29 mm
04719872149880E-XPE Patellar, on set, 3 pegs, X-small, Ø26 mm

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