Identity
- Trade Name
- Airtraq FDA UDI
- Generic Name
- Video intubation laryngoscope imaging system FDA UDI
- Device Name
- Max View Display FDA UDI
- Model / Reference
- A300 FDA UDI
- Description
- Max View Display FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00693602613008 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Video intubation laryngoscope imaging system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Video intubation laryngoscope imaging system
Airtraq by Prodol Meditec , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Video intubation laryngoscope imaging system.
- Airtraq — Prodol Meditec , Ltd. · Class I
- Airtraq — Prodol Meditec , Ltd. · Class I
- Airtraq — Prodol Meditec , Ltd. · Class I
- Airtraq — Prodol Meditec , Ltd. · Class I
- Airtraq — Prodol Meditec , Ltd. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Prodol Meditec , Ltd.
Sources (1)
- FDA UDI 96bae7b8-c4be-43d1-993f-a092cd4f13cc 33 fields · synced May 30, 2026