SoloMobile 9SOL2210

GUDID 05711665004009

Gamma Camera System

Ddd-Diagnostic A/S

Mobile gamma camera system
Primary Device ID05711665004009
NIH Device Record Key0d4dd789-23e1-4e4e-8e86-0ae1cd5ca72e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSoloMobile
Version Model NumberSoloMobile Gamma Camera System
Catalog Number9SOL2210
Company DUNS305116642
Company NameDdd-Diagnostic A/S
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9999999999
Emailsupport@ddd-diagnostic.dk

Device Dimensions

Weight252 Kilogram
Height173 Centimeter
Depth138 Centimeter
Width70 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS105711665004009 [Primary]

FDA Product Code

IYXCamera, Scintillation (Gamma)

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 Date2016-11-15

Devices Manufactured by Ddd-Diagnostic A/S

05711665003033 - QuantumCam2020-05-06 Gamma Camera System
05711665002012 - CardioMD2018-08-06 Gamma Camera System
05711665003019 - BodyMD2018-08-06 Gamma Camera System
05711665001008 - C.Cam2018-07-06 Gamma Camera System
05711665002005 - CorCam2018-07-06 Gamma Camera System
05711665002006 - CardioMD2018-07-06 Gamma Camera System
05711665003002 - QuantumCam2018-07-06 Gamma Camera System
05711665003003 - BodyMD2018-07-06 Gamma Camera System

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.