PRO-DENSE 12001500

GUDID 00889797998741

Guide Wire

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin Orthopaedic implant calibration pin
Primary Device ID00889797998741
NIH Device Record Key13aae140-ac98-49da-82b6-1cb958b6d661
Commercial Distribution StatusIn Commercial Distribution
Brand NamePRO-DENSE
Version Model Number12001500
Catalog Number12001500
Company DUNS807201207
Company NameWRIGHT MEDICAL TECHNOLOGY, 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 Datetrue
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)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com

Device Dimensions

Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch
Outer Diameter3.2 Millimeter
Length11 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100889797998741 [Primary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-08-15
Device Publish Date2016-09-17

On-Brand Devices [PRO-DENSE]

0084042019954610001200
00840420171306P7SM0404
00840420171290P7SM0402
00840420159786P7XS0404
0084042015973187XS0404
0084042015972487XS0402
0084042014079187SRIN04
0084042013730287SRCK15
0084042013729687SR0420
0084042013728987SR0410
0084042013727287SR0404
0084042012831712000400
0088979799876512001211
0088979799875812001216
0088979799872712001200
0088979799871012001208
0088979799870312001210
00889797998741Guide Wire

Trademark Results [PRO-DENSE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PRO-DENSE
PRO-DENSE
78956507 3350402 Live/Registered
Wright Medical Technology, inc.
2006-08-21

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