961682

GUDID 10603295239802

UNIVERSAL REVISION FEMORAL BROACH HANDLE

DEPUY ORTHOPAEDICS, INC.

Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting
Primary Device ID10603295239802
NIH Device Record Key0c085e0f-631f-4cab-b389-7bf445b06fae
Commercial Distribution StatusIn Commercial Distribution
Version Model Number96-1682
Catalog Number961682
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295239802 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

[10603295239802]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-05-13
Device Publish Date2018-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

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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
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