FDA UDI In Commercial Distribution 🇺🇸 United States

Fraxis Duo ARM

DI: 08800023200027 · Model: FRX 2.0 Articualed Arm · ILOODA.CO.,LTD
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fraxis Duo ARM
Primary DI
08800023200027
Version / Model
FRX 2.0 Articualed Arm
Company Name
ILOODA.CO.,LTD
Labeler DUNS
631129749
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-16
Public Version
5
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
ddacbc64-b893-4f11-9318-01be072b1581

Device Description

FRX 2.0 Articualed Arm

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
GEX Powered Laser Surgical Instrument
OUH Skin Resurfacing Rf Applicator

GMDN Terms

Code Name
44776 Electrosurgical system
61473 Dermatological carbon dioxide laser system

Identifiers

Type ID
Primary 08800023200027

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160312 000