Diagnostic Ultrasound System

GUDID 06971355421311

SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.

General-purpose ultrasound imaging system
Primary Device ID06971355421311
NIH Device Record Keya2086ca8-49ee-4ce6-89fc-822d4f1674ac
Commercial Distribution StatusIn Commercial Distribution
Brand NameDiagnostic Ultrasound System
Version Model NumberCarnation Pro
Company DUNS543063066
Company NameSHENZHEN WISONIC MEDICAL TECHNOLOGY 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 Datetrue
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
GS106971355421311 [Primary]

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 Date2023-10-19
Device Publish Date2023-10-11

On-Brand Devices [Diagnostic Ultrasound System]

06971355420932Clivia 90Go
06971355420925Clivia 90Plus
06971355420918Clivia 90Pro
06971355420901Clivia 90T
06971355420895Clivia 90
06971355420888Clivia 90Nova
06971355420871Clivia 90Exp
06971355420864Clivia 90Elite
06971355421335Carnation Fast
06971355421328Carnation Ultra
06971355421311Carnation Pro
06971355421304Carnation T
06971355421298Carnation
06971355421281Carnation Neo
06971355421274Carnation Exp
06971355421267Carnation+

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