Identity
- Trade Name
- Machined Medical Litter (AeroSled MA) FDA UDI
- Generic Name
- Ambulance stretcher, manual FDA UDI
- Device Name
- AEROSLED, MACHINED, TD WITH CG PLACARD FDA UDI
- Model / Reference
- AS1-061-01 FDA UDI
- Description
- AEROSLED, MACHINED, TD WITH CG PLACARD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810050862851 FDA UDI
- FDA Product Code
- FPP FDA UDI
- GMDN Term
- Ambulance stretcher, manual 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ambulance stretcher, manual
Machined Medical Litter (AeroSled MA) by Lifeport, Llc. — 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
- Lifeport, Llc.
Sources (1)
- FDA UDI ec7bfc14-e711-4163-a412-135abd308857 34 fields · synced May 30, 2026