FDA UDI In Commercial Distribution 🇺🇸 United States

Sectum Foot Switch

DI: 00850017374157 · Model: 300-1306 · NEAUVIA NORTH AMERICA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sectum Foot Switch
Primary DI
00850017374157
Version / Model
300-1306
Company Name
NEAUVIA NORTH AMERICA, INC.
Labeler DUNS
117030786
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-27
Public Version
1
Public Version Date
2021-10-05
Public Version Status
New
Public Device Record Key
70011f84-62d3-431c-8191-da4e3f47bcf2

Device Description

Foot switch for the Sectum System

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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
PBX Massager, Vacuum, Radio Frequency Induced Heat

GMDN Terms

Code Name
45219 Radio-frequency skin contouring system

Identifiers

Type ID
Primary 00850017374157

Premarket Submissions

Submission Number Supplement Number
K202780 000