FDA UDI In Commercial Distribution 🇺🇸 United States

L51K

DI: 04573596212134 · Model: L51K · FUJIFILM HEALTHCARE CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
L51K
Primary DI
04573596212134
Version / Model
L51K
Company Name
FUJIFILM HEALTHCARE CORPORATION
Labeler DUNS
680160734
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-18
Public Version
2
Public Version Date
2022-08-04
Public Version Status
Update
Public Device Record Key
990e68c8-7aab-43f4-9e5c-7b27166fa299

Device Description

Probe

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
Yes
Sterilization Methods
["Liquid Chemical", "Peracetic Acid", "Hydrogen Peroxide", "Ethylene Oxide"]

Product Codes

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

GMDN Terms

Code Name
40770 Surgical ultrasound imaging transducer

Identifiers

Type ID
Primary 04573596212134
Previous 04562122958820

Premarket Submissions

Submission Number Supplement Number
K163505 000