House-Type Piston & Wire

GUDID 00763000034887

PROSTHESIS 1117045 PISTON/WIRE 5.0 SST

MEDTRONIC XOMED, INC.

Ossicular prosthesis, partial
Primary Device ID00763000034887
NIH Device Record Key87d5586d-8726-4d40-a061-394b428ebc10
Commercial Distribution StatusIn Commercial Distribution
Brand NameHouse-Type Piston & Wire
Version Model Number1117045
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
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 Dimensions

Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000034887 [Primary]

FDA Product Code

ETAREPLACEMENT, OSSICULAR PROSTHESIS, TOTAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-18
Device Publish Date2023-12-08

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