FDA UDI In Commercial Distribution 🇺🇸 United States

UST-52114P-B

DI: 00860007188336 · Model: UST-52114P-B · Fujifilm Healthcare Americas Corporation
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
UST-52114P-B
Primary DI
00860007188336
Version / Model
UST-52114P-B
Company Name
Fujifilm Healthcare Americas Corporation
Labeler DUNS
603156043
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-01
Public Version
3
Public Version Date
2021-08-16
Public Version Status
Update
Public Device Record Key
c0edf81b-d44f-41be-ae53-73365de41b9b

Device Description

Ultrasound Brainpath Probe

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Hydrogen Peroxide

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic
ITX Transducer, Ultrasonic, Diagnostic
IYN System, Imaging, Pulsed Doppler, Ultrasonic

GMDN Terms

Code Name
40770 Surgical ultrasound imaging transducer

Identifiers

Type ID
Primary 00860007188336
Previous 00869047000424

Premarket Submissions

Submission Number Supplement Number
K122537 000