← Back to catalogue

Mvp®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
MVP® FDA UDI
Generic Name
Non-neurovascular embolization coil FDA UDI
Device Name
MICRO VASCULAR PLUG MVP-9Q V02 US FDA UDI
Model / Reference
MVP-9Q FDA UDI
Description
MICRO VASCULAR PLUG MVP-9Q V02 US FDA UDI

Identifiers

Primary DI / UDI-DI
00847536020832 FDA UDI
510(k) Number
K150108 FDA UDI
FDA Product Code
KRD FDA UDI
GMDN Term
Non-neurovascular embolization coil FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Non-neurovascular embolization coil

Mvp® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-neurovascular embolization coil.

Cleared under the same submission

K150108 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 9f7415f2-94ba-4599-a627-d5cbb7e25887 36 fields · synced May 30, 2026