FDA UDI In Commercial Distribution 🇺🇸 United States

Ultratone

DI: 05056119700008 · Model: Futura Pro (US Specification) · ULTRATONE SCIENTIFIC INSTRUMENTS LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ultratone
Primary DI
05056119700008
Version / Model
Futura Pro (US Specification)
Catalog Number
USFPC1
Company Name
ULTRATONE SCIENTIFIC INSTRUMENTS LIMITED
Labeler DUNS
226427250
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
31fe3727-752c-4519-9f18-62880b146221

Device Description

Futura Pro (US Specification) System comprising: Console, Body Applicator, and 1MHz Ultrasound Applicator.

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
IMG Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat

GMDN Terms

Code Name
17908 Physical therapy ultrasound/neuromuscular stimulation system

Identifiers

Type ID
Primary 05056119700008