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Airtraq Avant Disposable Blade Small + Eyecup
EUDAMEDFDA UDIClass I (EU MDR)
Ref A-521
Identity
- Trade Name
- Airtraq Avant Disposable Blade Small + Eyecup EUDAMEDAirtraq FDA UDI
- Generic Name
- Video intubation laryngoscope blade/handle shell FDA UDI
- Device Name
- Airtraq Video Laryngoscopes and accesories. EUDAMEDAirtraq Avant Small Blade FDA UDI
- Model / Reference
- A-521 EUDAMEDFDA UDI
- Description
- Airtraq Avant Small Blade FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08436031035216 EUDAMEDFDA UDI
- Basic UDI-DI
- 843603103PRODOLMEDKT EUDAMED
- FDA Product Code
- CCW FDA UDI
- EMDN Code
- R9002 LARYNGOSCOPE BLADES, SINGLE-USE EUDAMED
- GMDN Term
- Video intubation laryngoscope blade/handle shell FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 868.5540 FDA UDI
- Market of Registration
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Airtraq Avant Disposable Blade Small + Eyecup by Prodol Medited Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 843603103PRODOLMEDKT | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Prodol Medited Limited
- EUDAMED SRN
- CN-MF-000014746
- Authorised Representative
- Prodol Meditec S.A. ES-AR-000005064
Sources (2)
- EUDAMED f2af900c-8825-4e99-a4c3-bf5f40e7722f 61 fields · synced Jul 28, 2026
- FDA UDI ecc7094d-b0d8-447e-b7d9-aae74d50b5f0 33 fields · synced May 30, 2026