cV4 Diagnostic Ultrasound System

GUDID 08800289979132

cV4 Diagnostic Ultrasound System

SAMSUNG MEDISON CO., LTD.

General-purpose ultrasound imaging system
Primary Device ID08800289979132
NIH Device Record Keyfa203a65-1ab9-43c0-a0b6-436879d470ed
Commercial Distribution StatusIn Commercial Distribution
Brand NamecV4 Diagnostic Ultrasound System
Version Model NumbercV4
Company DUNS687785691
Company NameSAMSUNG MEDISON CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800289979132 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYNSystem, Imaging, Pulsed Doppler, Ultrasonic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-09-11
Device Publish Date2025-09-03

Devices Manufactured by SAMSUNG MEDISON CO., LTD.

08800289979132 - cV4 Diagnostic Ultrasound System2025-09-11cV4 Diagnostic Ultrasound System
08800289979132 - cV4 Diagnostic Ultrasound System2025-09-11 cV4 Diagnostic Ultrasound System
08800289981883 - cV5 Diagnostic Ultrasound System2025-09-11
08806167766030 - LA3-16AD2025-09-11
08809702988614 - MMPT3-72025-09-11
08809944884736 - TA2-92025-09-11
08809944906476 - LM2-18D2025-09-11
08809944935292 - MMPT3-72025-09-11
08809944942450 - miniER72025-09-11

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.