Leaf™ 66802119
by Smith & Nephew Medical, Ltd.
Leaf™ 66802119 is a Class I device made by Smith & Nephew Medical, Ltd., listed in FDA GUDID since 22 Feb 2022 (UDI-DI 05000223499907), registry data as of 22 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 | Number05000223499907 | Date22 Feb 2022 | StatusListed |
Official records
- AccessGUDID record 05000223499907
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Leaf™
- Generic name
- Wireless patient monitor/sensor reporting software, professional-only
- Model / Ref / Catalog
- 66802119
- Primary DI / UDI-DI
- 05000223499907
- FDA product code
- KMI
- GMDN term
- Wireless patient monitor/sensor reporting software, professional-only
- Device class
- Class I
- Regulation number
- 880.2400
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KMI (Monitor, Bed Patient).
- POSEY SITTER by J. T. Posey Co.
- JDM SP2 SENSOR by Jd Monitoring C/O Mackler, Cooper and Gibbs
- AMB-ALERT by MED WAY INC.
- BED-CHECK: II-IFAC by Bed-Check Corp.
- INFORMER PLUS by Microtech Medical, Inc.
- AMBULARM by Rigi Systems, Inc.
- MOBILECARE MONITOR, MODEL 2100 by Aframe Digital, Inc.
- THE MONITOR ELECTRONIC BED ALARM SYSTEM by The Monitor Corp.
- PM-PAGER by Hill Engineering
- LEAF PATIENT MONITORING SYSTEM by Leaf Healthcare, Inc.