V7

GUDID 08809725816864

SAMSUNG MEDISON CO., LTD.

General-purpose ultrasound imaging system
Primary Device ID08809725816864
NIH Device Record Keyb9f1b349-4214-4c95-a032-b1b9eeead852
Commercial Distribution StatusIn Commercial Distribution
Brand NameV7
Version Model NumberV7
Company DUNS687785691
Company NameSAMSUNG MEDISON CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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
GS108809725816864 [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 Date2022-07-20
Device Publish Date2022-07-12

Devices Manufactured by SAMSUNG MEDISON CO., LTD.

08809944937180 - HERA W10 Diagnostic Ultrasound System2024-12-16
08809944937371 - HERA W10 Diagnostic Ultrasound System2024-12-16
08809944937555 - HERA W9 Diagnostic Ultrasound System2024-12-16
08809944937746 - HERA W9 Diagnostic Ultrasound System2024-12-16
08809944937913 - HERA W9 Diagnostic Ultrasound System2024-12-16
08809944938088 - HERA W9 Diagnostic Ultrasound System2024-12-16
08809944938118 - HERA W10 Diagnostic Ultrasound System2024-12-16
08809944938262 - HERA W10 Diagnostic Ultrasound System2024-12-16

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