Reservoir

GUDID 00763000980849

RESERVOIR 24106 A NEONT ANGULAR CATH 3CM

MEDTRONIC POWERED SURGICAL SOLUTIONS

Cranial port/reservoir
Primary Device ID00763000980849
NIH Device Record Keyb6b784b8-16d7-416d-aa30-9c47c2eb482e
Commercial Distribution StatusIn Commercial Distribution
Brand NameReservoir
Version Model Number24106 A
Company DUNS098308849
Company NameMEDTRONIC POWERED SURGICAL SOLUTIONS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000980849 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LKGPort & catheter, implanted, subcutaneous, intraventricular

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


[00763000980849]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-08-11
Device Publish Date2025-08-03

On-Brand Devices [Reservoir]

00763000980856RES 22101 A NEO FLAT DOME W/ 3.0CM VCATH
00763000980849RESERVOIR 24106 A NEONT ANGULAR CATH 3CM

Trademark Results [Reservoir]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RESERVOIR
RESERVOIR
98758610 not registered Live/Pending
Carnot Labs, Inc.
2024-09-19
RESERVOIR
RESERVOIR
98465695 not registered Live/Pending
Reservoir Limited
2024-03-25
RESERVOIR
RESERVOIR
98048897 not registered Live/Pending
Reservoir Roasters, LLC
2023-06-19
RESERVOIR
RESERVOIR
97768983 not registered Live/Pending
Reservoir Distillery, LLC.
2023-01-26
RESERVOIR
RESERVOIR
97544747 not registered Live/Pending
RESERVOIR, LLC
2022-08-11
RESERVOIR
RESERVOIR
90149740 not registered Live/Pending
Flo Free LLC
2020-08-31
RESERVOIR
RESERVOIR
87853944 not registered Live/Pending
Jeffrey Court, Inc.
2018-03-28
RESERVOIR
RESERVOIR
87837870 5595057 Live/Registered
Carollo Engineers, Inc.
2018-03-16
RESERVOIR
RESERVOIR
87837853 5595056 Live/Registered
Carollo Engineers, Inc.
2018-03-16
RESERVOIR
RESERVOIR
87472758 5863544 Live/Registered
OFS Brands Inc.
2017-06-02
RESERVOIR
RESERVOIR
87004077 5090526 Live/Registered
RESERVOIR AND WOOD LLC
2016-04-18
RESERVOIR
RESERVOIR
86473575 not registered Dead/Abandoned
Aliza and Alissa, LLC
2014-12-08

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.