Primary Device ID | 00861334000339 |
NIH Device Record Key | 4fb5806e-95a3-4596-9232-be2def279281 |
Commercial Distribution Discontinuation | 2019-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | DoseLab Pro |
Version Model Number | 6.8.0 |
Catalog Number | DoseLab Pro |
Company DUNS | 009120817 |
Company Name | VARIAN MEDICAL SYSTEMS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com | |
Phone | 888-263-8541 |
support@mobiusmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00861334000339 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-07-16 |
Device Publish Date | 2016-09-14 |
08613340003003 | Dosimetry QA Software |
00861334000339 | Dosimetry QA Software |