Primary Device ID | 00850009343031 |
NIH Device Record Key | c7320fc6-a2b0-4e08-807a-a3558357bb9a |
Commercial Distribution Discontinuation | 2020-11-24 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MIMcloud |
Version Model Number | 2.12 |
Company DUNS | 136977290 |
Company Name | MIM SOFTWARE INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850009343031 [Primary] |
LMB | Device, Digital Image Storage, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-08-21 |
Device Publish Date | 2020-06-16 |
00850009343130 | MIMcloud is a service for institutions, clinicians, and patients provided for the purpose of sec |
00850009343031 | MIMcloud is a service for institutions, clinicians, and patients provided for the purpose of sec |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MIMCLOUD 87370063 5301172 Live/Registered |
MIM Software Inc. 2017-03-14 |