MDE001

GUDID 10603295262886

EXTRACTOR SLEEVE

DEPUY FRANCE

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable
Primary Device ID10603295262886
NIH Device Record Keyd7301740-26f6-4985-9635-6d1a5db52114
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberMDE001
Catalog NumberMDE001
Company DUNS502491434
Company NameDEPUY FRANCE
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
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295262886 [Primary]

FDA Product Code

HWBEXTRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


[10603295262886]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-04-23
Device Publish Date2018-09-24

Devices Manufactured by DEPUY FRANCE

10603295260660 - KAR2021-10-25 KAR Cementless Revision Femoral Stem with Collar KAR 16 12/14mm
10603295260677 - KAR2021-10-25 KAR Cementless Revision Femoral Stem with Collar KAR 18 12/14mm
10603295260684 - KAR2021-10-25 KAR Cementless Revision Femoral Stem with Collar KAR 20 12/14mm
10603295116615 - DELTA XTEND2020-04-06 DELTA Xtend CUP EXTRACTION CLAMP
10603295261452 - REEF2020-04-06 REEF
10603295261520 - REEF2020-04-06 REEF
10603295272908 - DELTA XTEND2020-01-21 DELTA XTEND REVERSE SHOULDER SYSTEM Cementless Metaglene +10mm HA COATED CEMENTLESS
10603295272915 - DELTA XTEND2020-01-21 DELTA XTEND REVERSE SHOULDER SYSTEM Cementless Metaglene +15mm HA COATED CEMENTLESS

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