FirstStep Select 203660
FirstStep Select 203660 is a low-air-loss bed (FDA Class II; FDA product code FNM, Mattress, Air Flotation, Alternating Pressure) made by Arjohuntleigh AB, listed in FDA GUDID since 1 Aug 2022 (UDI-DI 05055982784894), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05055982784894 | Date1 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 05055982784894
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- FirstStep Select
- Generic name
- Low-air-loss bed
- Model / reference
- 203660
- Primary DI / UDI-DI
- 05055982784894
- FDA product code
- FNM
- GMDN term
- Low-air-loss bed
- Device class
- Class II
- Regulation number
- 880.5550
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code FNM (Mattress, Air Flotation, Alternating Pressure).
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- PHYSIO/1000 by Physio Designs, Inc.
- PEGASUS MATTRESS by Dermalex Co.