FDA UDI In Commercial Distribution 🇺🇸 United States

ThermiRF+

DI: 00817371020618 · Model: ThermiRF+ · Thermi
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ThermiRF+
Primary DI
00817371020618
Version / Model
ThermiRF+
Company Name
Thermi
Labeler DUNS
021008486
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-05
Public Version
1
Public Version Date
2022-09-13
Public Version Status
New
Public Device Record Key
a694635f-d2ec-4270-aa50-5c90ace17939

Device Description

Thermi radio frequency 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
Yes
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary 00817371020618

Premarket Submissions

Submission Number Supplement Number
K173582 000