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AerVia Neonatal Supraglottic Airway Device, Variety
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- AerVia Neonatal Supraglottic Airway Device, Variety FDA UDI
- Generic Name
- Oropharyngeal airway, single-use FDA UDI
- Device Name
- AerVia Neonatal Supraglottic Airway Device, Variety [1 Small, 2 Medium, 2 Large, 1 X-Large] FDA UDI
- Model / Reference
- AVVariety FDA UDI
- Description
- AerVia Neonatal Supraglottic Airway Device, Variety [1 Small, 2 Medium, 2 Large, 1 X-Large] FDA UDI
Identifiers
- Catalog Number
- AVVariety FDA UDI
- Primary DI / UDI-DI
- 00361938122050 FDA UDI
- FDA Product Code
- CAE FDA UDI
- GMDN Term
- Oropharyngeal airway, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5110 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Oropharyngeal airway, single-use
AerVia Neonatal Supraglottic Airway Device, Variety by Ony Biotech Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Ony Biotech Inc.
Sources (1)
- FDA UDI 55245cc8-52ec-4a1e-bcac-547954c79e7e 36 fields · synced May 30, 2026