FDA UDI In Commercial Distribution 🇺🇸 United States

Revo MRI™ SureScan™

DI: 00643169493407 · Model: RVDR01 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revo MRI™ SureScan™
Primary DI
00643169493407
Version / Model
RVDR01
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-02-05
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
fc16215c-481c-421a-a96c-54f7afb0b2d3

Device Description

IPG RVDR01 Revo MRI SureScan US

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
LWP Implantable pulse generator, pacemaker (non-CRT)

GMDN Terms

Code Name
47265 Dual-chamber implantable pacemaker, rate-responsive

Identifiers

Type ID
Primary 00643169493407

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P090013 137
P090013 215

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 131 Degrees Fahrenheit