129901080

GUDID 10603295027072

CAS LIGAMENT TENSOR SIZE 2-XF

DEPUY INTERNATIONAL LTD

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation 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 Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID10603295027072
NIH Device Record Keyed89b3b6-396e-48d7-938a-8d834f0c191b
Commercial Distribution StatusIn Commercial Distribution
Version Model Number1299-01-080
Catalog Number129901080
Company DUNS896498813
Company NameDEPUY INTERNATIONAL LTD
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
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
GS110603295027072 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


[10603295027072]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2022-05-11
Device Publish Date2015-03-24

Devices Manufactured by DEPUY INTERNATIONAL LTD

10603295235958 - C-STEM2024-02-08 C-STEM END CAP
10603295235682 - C-STEM2024-02-05 C-STEM VOID CENTRALISER 10mm
10603295235736 - C-STEM2024-02-05 C-STEM VOID CENTRALISER 12mm
10603295235811 - C-STEM2024-02-05 C-STEM VOID CENTRALISER 14mm
10603295235873 - C-STEM2024-02-05 C-STEM VOID CENTRALISER 16mm
10603295235897 - C-STEM2024-02-05 C-STEM VOID CENTRALISER 18mm
10603295236351 - C-STEM2024-02-05 C-STEM CENTRALISER
10603295026969 - PATHWAY2023-10-27 PATHWAY TIBIAL SCREW 21mm

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