FDA device listing

Airtraq A-360 WiFi Camera (A-360),Airtraq A-390 WiFi Camera Accessories (A-390-ACC),Airtraq A-390 Wifi Camera Full KIT…

FDA device listing 1139002227 · PRODOL MEDITEC S.A.

Key facts

Proprietary names Airtraq A-360 WiFi Camera (A-360),Airtraq A-390 WiFi Camera Accessories (A-390-ACC),Airtraq A-390 Wifi Camera Full KIT (A-390-KIT),Airtraq A-390 WiWi Camera (A-390),Airtraq Avant Demo Optics (A-581),Airtraq Avant Docking station (A-590),Airtraq Avant Optics (A-501),Airtraq Avant Regular Blade (A-511),Airtraq Avant Small blade (A-521),Airtraq CAM APP,Airtraq Mobile APP,Airtraq Smartphone Adapter…
Owner/operator PRODOL MEDITEC S.A.
Owner/operator number 9079460
Product codes CCW
Device names CCW - Laryngoscope, Rigid
Device class Class I
Classification regulations (21 CFR) 868.5540
Review panels Anesthesiology
Registered establishments Prodol Meditec Limited, PRODOL MEDITEC S.A.
Establishment registrations 3005450700, 3007817051
FEI numbers 3005450700, 3007817051
Establishment operations Manufacturer, Specification Developer
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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