SONIALVISION G4

GUDID 04540217041022

SHIMADZU CORPORATION

Stationary general-purpose fluoroscopic x-ray system, digital
Primary Device ID04540217041022
NIH Device Record Keyd883840c-4467-4c70-bd89-b693d9eb9587
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONIALVISION G4
Version Model Number566-10000-41
Company DUNS690558747
Company NameSHIMADZU CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104540217041022 [Primary]

FDA Product Code

JAASystem, X-Ray, Fluoroscopic, Image-Intensified

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-05-28
Device Publish Date2019-08-14

On-Brand Devices [SONIALVISION G4]

04540217040964503-78000-27
04540217040957503-78000-26
04540217040926503-78000-23
04540217064816503-78000-54
04540217064809503-78000-24
04540217041060566-10000-47
04540217041053566-10000-46
04540217041046566-10000-43
04540217041039566-10000-42
04540217041022566-10000-41
04540217040896503-78000-53
04540217040889503-78000-52
04540217040872503-78000-51

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