Identity
- Trade Name
- Airo® FDA UDI
- Generic Name
- Full-body CT system FDA UDI
- Device Name
- AIRO® Computed Tomography (CT) X-ray System FDA UDI
- Model / Reference
- MobiCT-32 FDA UDI
- Description
- AIRO® Computed Tomography (CT) X-ray System FDA UDI
Identifiers
- Catalog Number
- MobiCT-32 FDA UDI
- Primary DI / UDI-DI
- 00869346000200 FDA UDI
- 510(k) Number
- K131431 FDA UDI
- FDA Product Code
- JAK FDA UDI
- GMDN Term
- Full-body CT system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1750 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
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Full-body CT system
Airo® by Mobius Imaging — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Mobius Imaging
Sources (1)
- FDA UDI 28e8914d-87ef-43cb-bbc5-fef818c7e858 37 fields · synced May 30, 2026