FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 06955139299990 · Model: ERA-G5-US · Acotec Scientific Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
06955139299990
Version / Model
ERA-G5-US
Company Name
Acotec Scientific Co., Ltd.
Labeler DUNS
548757551
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-21
Public Version
1
Public Version Date
2025-12-01
Public Version Status
New
Public Device Record Key
1d9be912-899a-4997-aada-5c5c43920139

Device Description

Endovenous Radiofrequency 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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary 06955139299990

Premarket Submissions

Submission Number Supplement Number
K250688 000