FDA UDI In Commercial Distribution 🇺🇸 United States

Falcon/Xpress

DI: 07290016880533 · Model: Falcon/Xpress · VIASONIX LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Falcon/Xpress
Primary DI
07290016880533
Version / Model
Falcon/Xpress
Company Name
VIASONIX LTD
Labeler DUNS
533070236
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-27
Public Version
1
Public Version Date
2025-01-06
Public Version Status
New
Public Device Record Key
d14af57d-2e6f-4609-965d-7b36d31f8222

Device Description

The Falcon/Xpress is intended for use in the noninvasive evaluation of peripheral vascular pathology in patients.

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
MR Unsafe
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
JOP Transducer, Ultrasonic

GMDN Terms

Code Name
40761 General-purpose ultrasound imaging system

Identifiers

Type ID
Primary 07290016880533

Premarket Submissions

Submission Number Supplement Number
K242662 000