Home GUDID 00854763006249 Acessa ProVu PFG Table Clamp
Primary DI 00854763006249
Brand Acessa ProVu PFG Table Clamp
Company ACESSA HEALTH INC.
Model MS-05-0257
Device description Field generator clamp assembly that connects the Planar Field generator to the hospital bed
Published 2018-10-11
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name HFG Coagulator, Laparoscopic, Unipolar (And Accessories) ITX Transducer, Ultrasonic, Diagnostic IYO System, Imaging, Pulsed Echo, Ultrasonic OEW Tracking, Soft Tissue, Intraoperative
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HFG Coagulator, Laparoscopic, Unipolar (And Accessories) Obstetrics/Gynecology 2 ITX Transducer, Ultrasonic, Diagnostic Radiology 2 IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology 2 OEW Tracking, Soft Tissue, Intraoperative Neurology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00854763006249 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00854763006249 00854763006249 854763006249 0854763006249
GMDN Terms# Term, Definition table Term Definition Radio-frequency ablation system An assembly of devices designed to generate and apply radio-frequency (RF) electrical current for heating via an electrode(s) in a precise location, at a controlled temperature, for focal ablation of non-cardiac tissues, including nerves, tumours, precancerous tissue; it may be intended for coagulation however it is not intended for electrosurgical cutting. It typically includes a mains electricity (AC-powered) RF current generator, controls, cables, and an appropriate electrosurgical ablation probe, catheter, and/or handpiece with electrode(s).
Regulatory Flags# DUNS number 080935394 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes#