10,000 results · 60ms · Sources: EU EUDAMED, US FDA

MODELS ERA 300 AND 3105 PACING SYSTEM ANALYZERS

FDA 510(k)
FDA Class 2 ·Cardiovascular

MODIFICATION TO ERA 300 DUAL CHAMBER PACING SYSTEM ANALYZER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SIEMENS-ELEMA PSA 376

FDA 510(k)
FDA Class 2 ·Cardiovascular

CARDIOTEST 2200

FDA 510(k)
FDA Class 2 ·Cardiovascular

MERLIN PSA PATIENT CABLE EX 3150, CABLE ADAPTER EX3170, M ADAPTER EX3180

FDA 510(k)
FDA Class 2 ·Cardiovascular

ERA 3000; PA-2 IS-1 ADAPTER; EK-4-N PACEMAKER TEST CABLE; ERA 3000 CHARGER; ERA 3000 BATTERY (TYPE 2); NK-11 POWER SUPP.

FDA 510(k)
FDA Class 2 ·Cardiovascular

Orantech

FDA UDI
Orantech Inc.·06941691975311·Mindray 6Pins Compatible, ESIS, 5-Lead, AHA, 0.6M

Orantech

FDA UDI
Orantech Inc.·06941691975274·Mindray-Datascope Compatible, ESIS,5-Lead, AHA,...

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·ATA SOFTWARE CARTRIDGE (SWM 1000 I-KTB.0.U)

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·BELOS VR-T ICD

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (ICD'S)

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·TEROX RV /KAINOX SL IMPLANTABLE CARDIOVERTER DEFIBRILLATOR/LEAD MODELS

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·BELOS VR ICD SYSTEM

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·BELOS VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·KENTROX RV-S/KENTROX SL-S ICD LEADS

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·KENTROX RV LEAD SYSTEMS

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·PHYLAX IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·KAINOX RV-S/ KAINOX VCS ICD LEADS

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval
FDA Class 2 ·KENTROX RV 65, KENTROX RV 75, KAINOX SL 65/13, KAINOX SL 65/18

CareLink SmartSync™

FDA UDI
MEDTRONIC, INC.·00763000688400·PRGM 24970A USA MKT BASE