Identity
- Trade Name
- 26P ProFlexx® FDA UDI
- Generic Name
- Ambulance stretcher, manual FDA UDI
- Device Name
- 26P ProFlexx®, Italian w/Mattress FDA UDI
- Model / Reference
- 0054208 FDA UDI
- Description
- 26P ProFlexx®, Italian w/Mattress FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190790000592 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Ambulance stretcher, manual FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6910 FDA UDI
- Commercial Distribution
- Not 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
No
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
26P ProFlexx® by Ferno-Washington, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Ferno-Washington, Inc.
Sources (1)
- FDA UDI b9dab81c-c2df-4d31-820b-83762b672b32 35 fields · synced Jun 9, 2026