Atlas Sensor Rev A
Atlas Sensor Rev A is a Class I device made by Atlas Lift Tech, Inc., listed in FDA GUDID since 14 Aug 2023 (UDI-DI 00860008806024), 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 | Number00860008806024 | Date14 Aug 2023 | StatusListed |
Official records
- AccessGUDID record 00860008806024
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Atlas Sensor
- Generic name
- Wireless patient monitor/sensor reporting software, professional-only
- Model / reference
- Rev A
- Primary DI / UDI-DI
- 00860008806024
- 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
- MRI safety
- MR Unsafe
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