Identity
- Trade Name
- Airtraq FDA UDI
- Generic Name
- Channelled video intubation laryngoscope FDA UDI
- Device Name
- Airtraq Avant Disposable Blade Small - Size 2 + Eyecup FDA UDI
- Model / Reference
- A-521 FDA UDI
- Description
- Airtraq Avant Disposable Blade Small - Size 2 + Eyecup FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00693602615217 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Channelled video intubation laryngoscope 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
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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: Channelled video intubation laryngoscope
Airtraq by Prodol Meditec , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Channelled video intubation laryngoscope.
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 45f16ee3-98e5-4674-beca-8b1252c03cb6 33 fields · synced May 30, 2026