Vehicle-monted option

GUDID 04547410354584

Optional parts to protect the FDR MS-3500 from vibration and shock when it is mounted on a vehicle.

FUJIFILM CORPORATION

Stationary mammographic x-ray system, digital
Primary Device ID04547410354584
NIH Device Record Keyf5125604-b2b6-4217-aaea-627ab2b7f440
Commercial Distribution StatusIn Commercial Distribution
Brand NameVehicle-monted option
Version Model NumberDR 3500 MBL KIT HA USA E
Company DUNS713565195
Company NameFUJIFILM 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 Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx
Phone+018002728465
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS104547410354584 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MUEFull field digital,system,x-ray,mammographic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-04-03

Devices Manufactured by FUJIFILM CORPORATION

14547410532873 - FUJIFILM2024-12-30 This hood is intended to be used in combination with compatible endoscopes to maintain the field of view during endoscopic proce
04547410515893 - FUJIFILM2024-10-14 This product is intended to be used in combination with the compatible endoscopes, camera head, light source and light guide to
04547410524284 - FUJIFILM2024-10-14 This product is intended to be used in combination with the compatible endoscopes, camera head, light source and light guide to
14547410500643 - FUJIFILM2024-09-30 FUJIFILM Endoscope Model EG-840N is intended for the visualization of the upper digestive tract, specifically for the observatio
04547410517330 - FUJIFILM2024-09-30 FUJIFILM Endoscope Model EG-840T, EG-840TP is intended for the visualization of the upper digestive tract, specifically for the
14547410528265 - FUJIFILM2024-09-30 FUJIFILM Endoscope Model EG-840T, EG-840TP is intended for the visualization of the upper digestive tract, specifically for the
04573596200704 - APERTO Lucent2024-09-27 Magnetic Resonance Diagnostic Device
04573596204368 - ECHELON Synergy2024-09-19 Magnetic Resonance Diagnostic Device

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