FDA UDI In Commercial Distribution 🇺🇸 United States

Vivid

DI: 00195278796462 · Model: T8 v208 · GE Medical Systems (China) Co.,Ltd.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Vivid
Primary DI
00195278796462
Version / Model
T8 v208
Company Name
GE Medical Systems (China) Co.,Ltd.
Labeler DUNS
654658731
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-06
Public Version
1
Public Version Date
2025-03-14
Public Version Status
New
Public Device Record Key
34062423-eb41-49d4-9e59-d80e4690244d

Device Description

T8 v208 console

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

GMDN Terms

Code Name
40763 Cardiovascular ultrasound imaging system

Identifiers

Type ID
Primary 00195278796462

Premarket Submissions

Submission Number Supplement Number
K243628 000