P.F.C. SIGMA LCS COMPLETE 217830126

GUDID 10603295094036

P.F.C. SIGMA LCS COMPLETE RP/PS INSERT TRIAL TRAY

DEPUY ORTHOPAEDICS, INC.

Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable
Primary Device ID10603295094036
NIH Device Record Key3ae225a4-5039-43c8-a1bc-686b57180ba0
Commercial Distribution StatusIn Commercial Distribution
Brand NameP.F.C. SIGMA LCS COMPLETE
Version Model Number2178-30-126
Catalog Number217830126
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
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
GS110603295094036 [Primary]

FDA Product Code

FSMTRAY, SURGICAL, INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


[10603295094036]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-07-08
Device Publish Date2018-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

10603295123132 - MORELAND2024-04-03 MORELAND REV INST SCREW TREPHINE REAMER 6.5mm
10603295123293 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 11mm 5.5 IN
10603295123309 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 12.5mm 5.5 IN
10603295123316 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 14mm 5.5 IN
10603295123323 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 15.5mm 5.5 IN
10603295123330 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 17mm 5.5 IN
10603295123347 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 18.5mm 5.5 IN
10603295123354 - MORELAND2024-04-03 MORELAND REV INST TREPHINE REAMER 11mm 9 IN

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