Drive D574P-1070J
Drive D574P-1070J is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 11 Feb 2020 (UDI-DI 00822383157801), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00822383157801 | Date11 Feb 2020 | StatusListed |
Official records
- AccessGUDID record 00822383157801
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Drive
- Generic name
- Patient transfer sliding board
- Model / reference
- D574P-1070J
- Description
- Part Patient Room Parts Product Description Armrest,D574,Jade,1/ea
- Primary DI / UDI-DI
- 00822383157801
- FDA product code
- KMN, INN
- GMDN term
- Patient transfer sliding board
- Device class
- Class I
- Regulation number
- 880.6140, 890.3100
- GUDID distribution status
- In Commercial Distribution
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