Truwave 896494023
Truwave 896494023 is a Class II device made by Edwards Lifesciences LLC, listed in FDA GUDID since 2 Jun 2023 (UDI-DI 00690103218503), 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 | Number00690103218503 | Date2 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 00690103218503
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Truwave
- Generic name
- General-purpose patient temperature probe, reusable
- Model / Ref / Catalog
- 896494023
- Primary DI / UDI-DI
- 00690103218503
- FDA product code
- DXO
- GMDN term
- General-purpose patient temperature probe, reusable
- Device class
- Class II
- Regulation number
- 870.2870
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 162.0000 Inch
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