FDA UDI In Commercial Distribution 🇺🇸 United States

LOGIQ

DI: 00195278111272 · Model: P9 R3 to R4 UPG · GE Ultrasound Korea Ltd.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LOGIQ
Primary DI
00195278111272
Version / Model
P9 R3 to R4 UPG
Company Name
GE Ultrasound Korea Ltd.
Labeler DUNS
690168810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-17
Public Version
2
Public Version Date
2022-08-25
Public Version Status
Update
Public Device Record Key
4b8a94b7-2021-4c53-8e12-ded91509c4d4

Device Description

LP9 R3 to R4 SW Conversion

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
40761 General-purpose ultrasound imaging system

Identifiers

Type ID
Primary 00195278111272

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K203114 000