FDA UDI In Commercial Distribution 🇺🇸 United States

Vivid

DI: 00840682123402 · Model: E v201 to v202 UPG · GE Vingmed Ultrasound AS
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vivid
Primary DI
00840682123402
Version / Model
E v201 to v202 UPG
Company Name
GE Vingmed Ultrasound AS
Labeler DUNS
518870571
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-11
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
6a4cd96b-10d5-4a21-9fba-f334499bb761

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYN System, imaging, pulsed doppler, ultrasonic
ITX Transducer, ultrasonic, diagnostic
IYO System, imaging, pulsed echo, ultrasonic

GMDN Terms

Code Name
40763 Cardiovascular ultrasound imaging system

Identifiers

Type ID
Primary 00840682123402

Premarket Submissions

Submission Number Supplement Number
K170823 000