FDA device listing

Disposable ECG Electrode ECG301,ECG302, ECG303, ECG304, ECG305, ECG306, ECG307, ECG308, ECG309, ECG310,ECG311, ECG312…

FDA device listing 1538950754 · Dongguan Quanding Medical Supplies Co., Ltd

Key facts

Proprietary names Disposable ECG Electrode ECG301,ECG302, ECG303, ECG304, ECG305, ECG306, ECG307, ECG308, ECG309, ECG310,ECG311, ECG312, ECG313, ECG314, ECG315, ECG316, ECG317, ECG318, ECG319, ECG320,ECG-A001, ECG-A002, ECG-A003, ECG-A004, ECG-A005, ECG-A006, ECG-A007, ECG-A008, ECG-A009, ECG-A010,ECG-A011, ECG-A012, ECG-A013, ECG-A014, ECG-A015, ECG-A016, ECG-A017, ECG-A018, ECG-A019, ECG-A020
Owner/operator Dongguan Quanding Medical Supplies Co., Ltd
Owner/operator number 10075777
Product codes DRX
Device names DRX - Electrode, Electrocardiograph
Device class Class II
Classification regulations (21 CFR) 870.2360
Review panels Cardiovascular
Registered establishments DONGGUAN QUANDING MEDICAL SUPPLIES CO., LTD
Establishment registrations 3017450375
FEI numbers 3017450375
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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