FDA UDI In Commercial Distribution 🇺🇸 United States

Visia AF MRI™ VR SureScan™

DI: 00643169929913 · Model: DVFB1D4 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Visia AF MRI™ VR SureScan™
Primary DI
00643169929913
Version / Model
DVFB1D4
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-12
Public Version
6
Public Version Date
2021-06-24
Public Version Status
Update
Public Device Record Key
04b739f1-6ac7-4a90-8c5c-a4329e126e79

Device Description

ICD VR DVFB1D4 VISIA MRI AF XT US DF4

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NVZ Pulse generator, permanent, implantable
LWS Implantable cardioverter defibrillator (non-CRT)

GMDN Terms

Code Name
35852 Single-chamber implantable defibrillator

Identifiers

Type ID
Primary 00643169929913

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 131 Degrees Fahrenheit