224510001

GUDID 10603295107606

GSRS BLUNT POINT GELPI RETRACTOR

DEPUY (IRELAND)

Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable
Primary Device ID10603295107606
NIH Device Record Key0937d5cb-5477-40e4-80a7-8e26ee506de9
Commercial Distribution StatusIn Commercial Distribution
Version Model Number2245-10-001
Catalog Number224510001
Company DUNS989365556
Company NameDEPUY (IRELAND)
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295107606 [Primary]

FDA Product Code

GADRETRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


[10603295107606]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-03-26
Device Publish Date2018-09-24

Devices Manufactured by DEPUY (IRELAND)

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10603295509202 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 28 MM +1.5 TRIAL HEAD
10603295509219 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 28 MM +5 TRIAL HEAD
10603295509226 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 28 MM +8.5 TRIAL HEAD
10603295509233 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 32 MM +1 TRIAL HEAD
10603295509240 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 32 MM +5 TRIAL HEAD
10603295509257 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 32 MM +9 TRIAL HEAD
10603295509264 - DEPUY SYNTHES2024-04-09 DEPUY SYNTHES 32 MM +13 TRIAL HEAD

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