PROSTALAC 254141000

GUDID 10603295129530

PROSTALAC MOLD BASE

DEPUY ORTHOPAEDICS, INC.

Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID10603295129530
NIH Device Record Key7d0c0200-753c-44e4-9e64-c2de6e176374
Commercial Distribution StatusIn Commercial Distribution
Brand NamePROSTALAC
Version Model Number2541-41-000
Catalog Number254141000
Company DUNS080506581
Company NameDEPUY ORTHOPAEDICS, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295129530 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


[10603295129530]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-05-03
Device Publish Date2018-09-24

On-Brand Devices [PROSTALAC]

10603295129714PROSTALAC HIP EXTRACTOR
10603295129554PROSTALAC QUICK RELEASE NUT
10603295129547PROSTALAC MOLD JAW
10603295129530PROSTALAC MOLD BASE

Trademark Results [PROSTALAC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PROSTALAC
PROSTALAC
75098179 2249944 Live/Registered
DEPUY SYNTHES, INC.
1996-05-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.