3D Imaging C-Arm Table, 115V 058-820

GUDID 00879942070514

The 3D Imaging C-Arm Table 820 is designed and equipped for use with 3D imaging rings and 3D C-Arms for general C-Arm and O-Arm applications. The table features motorized actuation of height, X-Y, lateral roll and Trendelenburg motions of the tabletop.

Mirion Technologies (capintec), Inc.

Fluoroscopy/angiography table, powered
Primary Device ID00879942070514
NIH Device Record Keyadbc4ec2-9693-42ec-8995-93a41be55fc4
Commercial Distribution StatusIn Commercial Distribution
Brand Name3D Imaging C-Arm Table, 115V
Version Model Number058-820
Catalog Number058-820
Company DUNS047684501
Company NameMirion Technologies (capintec), Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com
Phone201-825-9500
Emailcapintec@mirion.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100879942070514 [Primary]

FDA Product Code

FQOTable, Operating-Room, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-04
Device Publish Date2023-06-26

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