FDA UDI In Commercial Distribution 🇺🇸 United States

ScanPoint®

DI: 00879123004239 · Model: ScanPoint Local Client · VERATHON INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ScanPoint®
Primary DI
00879123004239
Version / Model
ScanPoint Local Client
Catalog Number
0900-1009
Company Name
VERATHON INC
Labeler DUNS
130598584
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d96e04b0-6db3-4e5c-a4fd-25164770632f

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

GMDN Terms

Code Name
40873 Ultrasound imaging system application software

Identifiers

Type ID
Primary 00879123004239

Premarket Submissions

Submission Number Supplement Number
K022153 000
K071217 000