Primary Device ID | SNMR05000521200 |
NIH Device Record Key | 6dc4ec69-82b6-49dc-9ba0-a43b966b965c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VISICOIL MR |
Version Model Number | SNMR-050-005-2120 |
Catalog Number | SNMR-050-005-2120 |
Company DUNS | 036545713 |
Company Name | Radiomed Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com | |
Phone | +1 901-432-7202 |
visicoil@izimed.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | SNMR05000521200 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2022-05-13 |