N/A 299966952

GUDID 10603295548980

MAKE TO ORDER ACS CUP IMPACTOR ASSEMBLY 13 INCH

DEPUY ORTHOPAEDICS, INC.

Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable
Primary Device ID10603295548980
NIH Device Record Key9d645437-f0ee-4919-8c01-6e43951c838a
Commercial Distribution StatusIn Commercial Distribution
Brand NameN/A
Version Model Number299966952
Catalog Number299966952
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295548980 [Primary]

FDA Product Code

HWAIMPACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


[10603295548980]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-08
Device Publish Date2023-11-30

On-Brand Devices [N/A]

10603295505914MAKE TO ORDER Tibial Rasp Pressure Bushing
10603295505907MAKE TO ORDER Tibial Rasp Fine 0 Degree Assembly
10603295548980MAKE TO ORDER ACS CUP IMPACTOR ASSEMBLY 13 INCH
10603295549086MAKE TO ORDER ARTICULAR CARTILAGE PASTE GRAFT REAMER 8MM

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