Identity
- Trade Name
- HYDROAIRE FDA UDI
- Generic Name
- Air-fluidized bed FDA UDI
- Device Name
- HOME USE FDA UDI
- Model / Reference
- 3000 FDA UDI
- Description
- HOME USE FDA UDI
Identifiers
- Catalog Number
- 4200002HU FDA UDI
- Primary DI / UDI-DI
- B2844200002HU1 FDA UDI
- FDA Product Code
- INX FDA UDI
- GMDN Term
- Air-fluidized bed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5160 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Air-fluidized bed
Hydroaire by Aurora Manufacturing, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- HYDROAIRE — AURORA MANUFACTURING, LLC. · Class II
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
- Aurora Manufacturing, Llc.
Sources (1)
- FDA UDI 4fd10ea0-2b5b-45fd-a5ea-9a20f6c4094c 34 fields · synced Jun 8, 2026