Identity
- Trade Name
- HYBRIBOARD FDA UDI
- Generic Name
- Portable stretcher FDA UDI
- Device Name
- The sides of the Hybriboard do not expose the patient to the risk of secondary damage caused, as is the case with basket stretchers, by the vertical walls of the stretcher being 20-25cm high. FDA UDI
- Model / Reference
- SPORT FDA UDI
- Description
- The sides of the Hybriboard do not expose the patient to the risk of secondary damage caused, as is the case with basket stretchers, by the vertical walls of the stretcher being 20-25cm high. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08057592700087 FDA UDI
- FDA Product Code
- FPP FDA UDI
- GMDN Term
- Portable stretcher FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6900 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
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Portable stretcher
Hybriboard by Flamor Srl — 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
- Flamor Srl
Sources (1)
- FDA UDI 6459473f-e27f-49be-88c8-1e3ba0e314f9 33 fields · synced Jun 8, 2026