VISIONAIRE GENESIS II V0200012

GUDID 00885556583029

NON STERILE VISIONAIRE LEFT CUTTING BLOCK KIT - GENESIS II

Smith & Nephew, Inc.

Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable
Primary Device ID00885556583029
NIH Device Record Key1c20940d-c7bd-42a4-9dc5-c9b5a7c3d5ab
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISIONAIRE GENESIS II
Version Model NumberV0200012
Catalog NumberV0200012
Company DUNS109903521
Company NameSmith & Nephew, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100885556583029 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


[00885556583029]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-30

On-Brand Devices [VISIONAIRE GENESIS II]

00885556583036NON STERILE VISIONAIRE RIGHT CUTTING BLOCK KIT - GENESIS II
00885556583029NON STERILE VISIONAIRE LEFT CUTTING BLOCK KIT - GENESIS II
00885556583012NON STERILE VISIONAIRE PROXIMAL TIBIA CUTTING BLOCK - GENESI
00885556583005NON STERILE VISIONAIRE DISTAL FEMUR CUTTING BLOCK - GENESIS
00885556076712VISIONAIRE PROXIMAL TIBIA CUTTING BLOCK - GENESIS II
00885556076354VISIONAIRE DISTAL FEMUR CUTTING BLOCK - GENESIS II
03596010653123VISIONAIRE RIGHT CUTTING BLOCK KIT - GENESIS II
03596010653116VISIONAIRE LEFT CUTTING BLOCK KIT - GENESIS II

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