FDA UDI In Commercial Distribution 🇺🇸 United States

IonicRF™

DI: 05415067029317 · Model: RFG-IONIC · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IonicRF™
Primary DI
05415067029317
Version / Model
RFG-IONIC
Catalog Number
RFG-IONIC
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-14
Public Version
3
Public Version Date
2023-10-26
Public Version Status
Update
Public Device Record Key
dc291efb-e0e7-4dd1-8f1c-f5450fe4d475

Device Description

Generator

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXD Generator, lesion, radiofrequency

GMDN Terms

Code Name
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary 05415067029317

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201610 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-30 – 60 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Handling Environment Temperature
Temperature Range
-30 – 60 Degrees Celsius