FDA UDI In Commercial Distribution 🇺🇸 United States

MVP™

DI: 00763000307790 · Model: MVP-5Q · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MVP™
Primary DI
00763000307790
Version / Model
MVP-5Q
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-31
Public Version
1
Public Version Date
2021-06-08
Public Version Status
New
Public Device Record Key
911222ca-278d-4b59-ad2c-723bdc232469

Device Description

PLUG MVP-5Q MICRO VASCULAR

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRD Device, Vascular, for Promoting Embolization

GMDN Terms

Code Name
60941 Non-neurovascular embolization coil

Identifiers

Type ID
Primary 00763000307790

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K141313 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.0 - 5.0 mm Vessel Diameter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid exposing the MVP system to water, sunlight, extreme temperatures, and high humidity during storage. Store the MVP system under controlled room temperature.
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry