FDA UDI In Commercial Distribution 🇺🇸 United States

MVP®

DI: 00847536027732 · Model: MVP-9Q · Reverse Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MVP®
Primary DI
00847536027732
Version / Model
MVP-9Q
Company Name
Reverse Medical Corporation
Labeler DUNS
963324913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-16
Public Version
6
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
157bb962-1eef-4518-99df-4e1145ac2a1b

Device Description

MICRO VASCULAR PLUG MVP-9Q V03 US EU

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 00847536027732

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150108 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid exposure to water, sunlight, extreme temperatures and high humidity during storage. Store the MVP System under controlled room temperature.