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Sign in to claim this brandProdol Meditec , Ltd.
US
Last updated May 23, 2026
What Prodol Meditec , Ltd. makes
Prodol Meditec, Ltd. manufactures channelled video intubation laryngoscopes, including video blade/handle shells and imaging systems for visualising the airway during intubation. Their portfolio also includes battery chargers for noninvasive medical devices.
The company’s devices are classified as Class I under FDA regulations and are listed via 510(k) and UDI registrations. Prodol Meditec, Ltd. is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Prodol Meditec, Ltd. manufacture?
Prodol Meditec, Ltd. specializes in devices related to airway management, specifically channelled video intubation laryngoscopes. These include video blade/handle shells, imaging systems for visualising the airway during intubation, and battery chargers designed for noninvasive medical devices. Their focus is on improving visualisation and ease of use during intubation procedures.
Where is Prodol Meditec, Ltd. based?
Prodol Meditec, Ltd. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with US-based medical device standards.
How are Prodol Meditec, Ltd.’s devices classified under FDA regulations?
Prodol Meditec, Ltd.’s devices are classified as Class I under FDA regulations. This classification is typically assigned to low-risk medical devices, though compliance with FDA requirements—such as 510(k) clearances and Unique Device Identification (UDI) registration—remains mandatory to ensure safety and performance.
Which regulatory registries or databases list Prodol Meditec, Ltd.’s devices?
Prodol Meditec, Ltd.’s devices are listed in the FDA’s 510(k) Premarket Notification database and the FDA’s Unique Device Identifier (UDI) registry. These registries confirm that the devices have undergone the necessary regulatory processes to demonstrate compliance with FDA requirements before entering the market.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (34)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Airtraq | A-051 | FDA UDI | Class I | Active |
| Airtraq | A609 | FDA UDI | Class I | Active |
| Airtraq | A6C3 | FDA UDI | Class I | Active |
| Airtraq | A6C2 | FDA UDI | Class I | Active |
| Airtraq | A-021 | FDA UDI | Class I | Active |
| Airtraq | A691 | FDA UDI | Class I | Active |
| Airtraq | A6C0 | FDA UDI | Class I | Active |
| Airtraq | A-041 | FDA UDI | Class I | Active |
| Airtraq | A681 | FDA UDI | Class I | Active |
| Airtraq | A690 | FDA UDI | Class I | Active |
| Airtraq | A6HA | FDA UDI | Class I | Active |
| Airtraq | A-390 | FDA UDI | Class I | Active |
| Airtraq | A-511 | FDA UDI | Class I | Active |
| Airtraq | A600 | FDA UDI | Class I | Active |
| Airtraq | A-590 | FDA UDI | Class I | Active |
| Airtraq | A-061 | FDA UDI | Class I | Active |
| Airtraq | A-501 | FDA UDI | Class I | Active |
| Airtraq | A-011 | FDA UDI | Class I | Active |
| Airtraq | A-521 | FDA UDI | Class I | Active |
| Airtraq | A-071 | FDA UDI | Class I | Active |
| Airtraq | A680 | FDA UDI | Class I | Active |
| Airtraq | A6M1 | FDA UDI | Class I | Active |
| Airtraq | A300 | FDA UDI | Class I | Active |
| Airtraq | A692 | FDA UDI | Class I | Active |
| Airtraq | A6M3 | FDA UDI | Class I | Active |
| Airtraq | A-390-KIT | FDA UDI | Class I | Active |
| Airtraq | A6M2 | FDA UDI | Class I | Active |
| Airtraq | A-031 | FDA UDI | Class I | Active |
| Airtraq | A620 | FDA UDI | Class I | Active |
| Airtraq | A-051 | FDA UDI | Class I | Active |
| Airtraq | A6M4 | FDA UDI | Class I | Active |
| Airtraq | A6C1 | FDA UDI | Class I | Active |
| Airtraq | A630 | FDA UDI | Class I | Active |
| Airtraq Sp Airtraq Avant | K121378 | FDA 510(k) | Class I | Active |
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