GUDID 00681490033343

PROSTHESIS 1112080 H/A TOTAL 90 ROUND

MEDTRONIC XOMED, INC.

Ossicular prosthesis, total
Primary Device ID00681490033343
NIH Device Record Key79816924-802a-4e90-9577-1e14598a705c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number1112080
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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
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
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

Length8 Millimeter
Length8 Millimeter
Length8 Millimeter
Length8 Millimeter
Length8 Millimeter
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length8 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100681490033343 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETAREPLACEMENT, OSSICULAR PROSTHESIS, TOTAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-06-19

Devices Manufactured by MEDTRONIC XOMED, INC.

00763000548797 - Hydrodebrider2026-02-23 HYDRODEBRIDER 1914001 STD HANDPIECE ROHS
00763000548803 - Hydrodebrider2026-02-23 HANDPIECE 1921002 HYDRODEBRID FRNTL ROHS
20763000888910 - Merocel2026-02-23 PACKING 400151 100PK MICRO SPHERES 4MM
20763000888927 - Merocel2026-02-23 PACKING 400152 100PK MICRO SPHERES 5MM
00763000956028 - Tubing Set2026-02-23 IRRIG SET 3318604E IPC SUCTION W/RC
00643169547087 - NIM®2025-09-22 MAINFRAME 8253402 NEURO 3.0 INTL EL ROHS
00763000745080 - NuVent™2025-08-25 INFLATOR KIT 18INFKIT BALLOON
00763000831479 - NIM™2025-08-19 PROBE NIMDTP35 ENDO 35CM 1MM BALL TIP

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.