MVP®

GUDID 00847536003637

PLUG MICRO VASCULAR MVP-7Q

Reverse Medical Corporation

Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil
Primary Device ID00847536003637
NIH Device Record Key1878c819-4eb3-4a70-bdb6-6a1b5e00f837
Commercial Distribution StatusIn Commercial Distribution
Brand NameMVP®
Version Model NumberMVP-7Q
Company DUNS963324913
Company NameReverse Medical Corporation
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

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to water, sunlight, extreme temperatures and high humidty. Store under controlled room temperature

Device Identifiers

Device Issuing AgencyDevice ID
GS100847536003637 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KRDDevice, Vascular, for Promoting Embolization

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


[00847536003637]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-06-17
Device Publish Date2015-10-23

On-Brand Devices [MVP®]

00847536027732MICRO VASCULAR PLUG MVP-9Q V03 US EU
00847536025431VASCULAR PLUG MVP-7Q MECHANICAL 7MM V03
00847536020832MICRO VASCULAR PLUG MVP-9Q V02 US
00847536004351MVP-5Q MICRO VASCULAR PLUG
00847536004344MVP-3Q MICRO VASCULAR PLUG
00847536004009MVP-9Q MICRO VASCULAR PLUG
00847536003637PLUG MICRO VASCULAR MVP-7Q
00847536003620MVP-5Q MICRO VASCULAR PLUG
00847536003613MVP-3Q MICRO VASCULAR PLUG
00847536003606MVP-5US MICRO VASCULAR PLUG
00847536003583MVP-3US MICRO VASCULAR PLUG
00847536020825VASCULAR PLUG MVP-7Q MECHANICAL 7MM V02

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