VISICOIL MR SNMR-050-005-2120

GUDID SNMR05000521200

0.50mm x 01.0cm VISICOIL MR Platinum loaded in an 21 gauge 20cm pre-waxed needle.

Radiomed Corporation

Radiological image marker, implantable
Primary Device IDSNMR05000521200
NIH Device Record Key6dc4ec69-82b6-49dc-9ba0-a43b966b965c
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISICOIL MR
Version Model NumberSNMR-050-005-2120
Catalog NumberSNMR-050-005-2120
Company DUNS036545713
Company NameRadiomed Corporation
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com
Phone+1 901-432-7202
Emailvisicoil@izimed.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCSNMR05000521200 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, Linear, Medical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-09-18
Device Publish Date2022-05-13

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