FDA UDI In Commercial Distribution 🇺🇸 United States

The Oligio

DI: 08800022305310 · Model: The Oligio · WONTECH CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
The Oligio
Primary DI
08800022305310
Version / Model
The Oligio
Company Name
WONTECH CO.,LTD
Labeler DUNS
695658263
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-17
Public Version
2
Public Version Date
2023-03-01
Public Version Status
Update
Public Device Record Key
4f8db561-655a-4d0a-868b-667802ff1eb9

Device Description

Radio Frequency Therapy System

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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
45219 Radio-frequency skin contouring system

Identifiers

Type ID
Primary 08800022305310

Premarket Submissions

Submission Number Supplement Number
K221989 000