MicroPort CRM S.r.l.

FDA Device Registration & Listing · Saluggia (VC) Vercelli, IT · Registration 1000165971

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1000165971
FEI Number
1000165971
Entity Name
MicroPort CRM S.r.l.
City/State/Country
Saluggia (VC) Vercelli, IT
Establishment Address
Via Crescentino s.n, Saluggia (VC) Vercelli 13040, IT
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
MicroPort CRM S.R.L. (Owner Number: 9059364)
Owner / Operator Contact Address
5677 Airline Road, Regulatory Affairs, c/o Dwyndl Nelms, Arlington, TN 38002, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Magnet Paradym RF DR 9550 Paradym RF VR 9250 INTENSIA VR 124 INTENSIA DR 154 SMARTVIEW Hotspot Brady Remote Monitoring System PLATINIUM DR 1510 PLATINIUM VR 1240 PLATINIUM VR 1210 PLATINIUM DR 1540 Orchestra Plus Programmer Orchestra Programmer Paradym DR 8550 Paradym VR 8250 Smart Monitor (home monitor) CPR4 Remote Monitoring Software SmartTouch Programmer Software (SmartView) Reply DR Accessory for pacemaker, ICD and CRT-D Permanent magnet Esprit SR Reply SR Esprit DR Accessory for pacemaker, ICD and CRT-D Screw driver SMARTVIEW Hotspot Brady Remote Monitoring System CPR3 telemetry wand (Accessory to SmartView Hotspot) CPR4BR telemetry wand (Accessory to Smart Spot) Smart Spot (Brady home monitor) ALIZEA DR 1600 CELEA DR 1400 ALIZEA SR 1300 CELEA SR 1100 SmartView Connect App (V1) FLEXIGO Slitter SMARTVIEW Home Monitor Paradym RF CRT-D Model 9750 Paradym CRT-D Model 8750 INTENSIA CRT-D 174 PLATINIUM CRT-D 1741 SMARTVIEW Hotspot Brady Remote Monitoring System PLATINIUM CRT-D 1711 ORCHESTRA Plus Link PLATINIUM 4LV CRT-D 1744 Smart Monitor (home monitor) SpiderView

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DTG Magnet, Test, Pacemaker Cardiovascular Class 1 870.3690 2021-09-21
MRM Defibrillator, Implantable, Dual-Chamber Unknown Class 3 N/A 2009-08-31
OSR Pacemaker/Icd/Crt Non-Implanted Components Unknown Class 3 N/A 2009-08-31
LWS Implantable Cardioverter Defibrillator (Non-Crt) Unknown Class 3 N/A 2009-08-31
DXY Implantable Pacemaker Pulse-Generator Cardiovascular Class 3 870.3610 2009-08-31
LWP Implantable Pulse Generator, Pacemaker (Non-Crt) Unknown Class 3 N/A 2009-08-21
DXY Implantable Pacemaker Pulse-Generator Cardiovascular Class 3 870.3610 2009-08-21
NVZ Pulse Generator, Permanent, Implantable Unknown Class 3 N/A 2009-08-21
DWS Instruments, Surgical, Cardiovascular Cardiovascular Class 1 870.4500 2025-06-30
LWS Implantable Cardioverter Defibrillator (Non-Crt) Unknown Class 3 N/A 2009-08-26
DXY Implantable Pacemaker Pulse-Generator Cardiovascular Class 3 870.3610 2009-08-26
OSR Pacemaker/Icd/Crt Non-Implanted Components Unknown Class 3 N/A 2009-08-26
NIK Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D) Unknown Class 3 N/A 2009-08-26
MWJ Electrocardiograph, Ambulatory (Without Analysis) Cardiovascular Class 2 870.2800 2011-01-14

Official Correspondent

John Skousen

US Agent Details

John Skousen Business: MicroPort CRM Email: john.skousen@crm.microport.com Phone: (801) 3864437

Related Public Records

Same Entity

MicroPort CRM S.R.L.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K854482 Medtronic Vascular ALTERNATE STERILE PKG IMPLANTABLE PULSE GENERATORS 1986-02-28
K790690 Cordis Corp. OMNI-STANICOR-(THETA) MODEL 217 1979-05-16

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0033-2018 St Jude Medical Inc. 3
Merlin@Home Software Model EX2000 v8.2.2 for Merlin@Home Transmitter Models EX1150, EX1150W, EX1100, and EX1100W. The Merlin@home Transmitters are a component of St. Jude Medicals (SJM) Remote Care System. These Merlin@home transmitters are used to retrieve information from the SJM implantable medical device (IMD) using RF telemetry. The data is then sent back to the Merlin.net Patient Care Network through a built-in modem or, alternatively, through a USB cellular adapter or a USB based Broadband Kit. The transmitted data enables clinicians to remotely monitor a patients IMD using a secure, encrypted, password-protected web site, thus reducing the number of in-clinic visits a patient needs to make to their physician. The transmitter monitors the patients device daily between scheduled follow-ups and can alert a clinician if it detects anything out of the norm.
Z-0002-2007 Guidant Corporation 3
Guidant Zoom Latitude Programming System, Model 3120, Programmer/Recorder/Monitor (PRM). A portable cardiac rhythm management system designed to be used with Guidant implantable pulse generators. Guidant Corporation, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA.
Z-0003-2018 St Jude Medical Inc. 3
Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q; Fortify ST VR, Model Numbers: CD1241-40 and CD1241-40Q; Fortify Assura VR, Model Numbers: CD1257-40, CD1257-40Q, CD1357-40C, CD1357-40Q; Fortify Assura ST VR, Model Numbers: CD1263-40, CD1263-40Q, CD1363-40C, CD1363-40Q; Fortify DR, Model Numbers: CD2231-40 and CD2231-40Q; Fortify ST DR, Model Numbers: CD2241-40 and CD2241-40Q; Fortify Assura DR, Model Numbers: CD2257-40, CD2257-40Q, CD2357-40C, CD2357-40Q; Fortify Assura ST DR, Model Numbers: CD2263-40, CD2263-40Q, CD2363-40C, CD2363-40Q Product Usage Fortify and Fortify Assura implantable cardioverter defibrillators (ICDS) are intended to provided ventricular anti-tachycardia pacing and ventricular defibrillation for automated treatment of life threatening ventricular arrhythmias. The devices may also be programmed to provide single or dual chamber bradycardia pacing
Z-0037-2012 Boston Scientific CRM Corp 3
LATITUDE Paceart Integration Software, version 1.00 Model 6472. LATITUDE Paceart Integration is software and therefore does not have any serial numbers. However, the software version affected is version 1.00 and is distributed on USB pen drives. These pen drives are lot number controlled and denoted as Model 6493. When used in conjunction with the LATITUDE EMR Integration software transfers data files from the Boston Scientific LATITUDE Patient Management system to a clinic's Paceart system.
Z-0030-2018 St Jude Medical Inc. 3
Assurity Model Numbers: PM1240, PM2240; Assurity + Model Number: PM2260; Accent Model Numbers: PM1210, PM2210, PM1222, PM2212; Accent MRI Model Numbers: PM1224, PM2218, PM2224 Implantation of a single-chamber pulse generator, dual-chamber pulse generator, or CRT-P is indicated in one or more of the following permanent conditions: Syncope, Presyncope, Fatigue, Disorientation, Or any combination of those symptoms. Implantation of a CRT-P is indicated for: Maintaining synchrony of the left and right ventricles in patients who have undergone an AV nodal ablation for chronic atrial fibrillation and have NYHA Class II or III heart failure. The reduction of the symptoms of moderate to severe heart failure (NYHA Class III or IV) in those patients who remain symptomatic despite stable, optimal medical therapy, and have a left ventricular ejection fraction d35% and a prolonged QRS duration

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000165971. Last updated year: 2026. Please use registration number 1000165971 when referencing this establishment in official correspondence.
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