Leaf™ 66802118
by Smith & Nephew Medical, Ltd.
Leaf™ 66802118 is a Class I device made by Smith & Nephew Medical, Ltd., listed in FDA GUDID since 22 Feb 2022 (UDI-DI 05000223499891), 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 | Number05000223499891 | Date22 Feb 2022 | StatusListed |
Official records
- AccessGUDID record 05000223499891
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- Withdrawn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
- 66802118
- Primary DI / UDI-DI
- 05000223499891
- 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).
- DYNASENSE SYSTEM by Centauri Medical, Inc.
- HOME AMB-ALERT by MED WAY INC.
- ULTIMAT-SENSOR FOR BED OCCUPANCY MONITOR by Ultimate Development Corp.
- BED PATIENT MONITOR by Clearview Electronics Corp.
- THE CELL CARE SYSTEM by The Clell Corp.
- INTEL-GE CARE INNOVATIONS QUIETCARE by Intel-Ge Care Innovations, LLC
- WANDER CARE by Care Electronics, Inc.
- SENIOR TECH TABS 88 TRANS RA1/WRA1/R1 ANN TYPE CR1 by Senior Technologies, Inc.
- RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR by Tactilitics, Inc.
- BED PATIENT PRESENCE MONITOR by Human Technologies, Inc.