N/A

GUDID 00763000247331

HAMMER 9734592 SLAP

MEDTRONIC POWERED SURGICAL SOLUTIONS

Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet Surgical mallet
Primary Device ID00763000247331
NIH Device Record Keya56de853-0810-4835-9a06-7b8bdac2d933
Commercial Distribution StatusIn Commercial Distribution
Brand NameN/A
Version Model Number9734592
Company DUNS098308849
Company NameMEDTRONIC POWERED SURGICAL SOLUTIONS
Device Count1
DM Exempttrue
Pre-market Exemptfalse
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000247331 [Primary]

FDA Product Code

FZYHAMMER, SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


[00763000247331]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-04
Device Publish Date2020-12-27

On-Brand Devices [N/A]

00763000247331HAMMER 9734592 SLAP
00763000585273TOOL 31AC75 LEGEND 31CM ACORN 7.5MM WING
00763000585266TOOL MR8-31AC75W MR8 31CM ACRN 7.5MM WNG

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