Probe Navigator C02 500
Probe Navigator C02 500 is a Class I device made by Z-Medical GmbH + Co. KG, listed in FDA GUDID since 17 Jan 2020 (UDI-DI 04057217005829), 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 | Number04057217005829 | Date17 Jan 2020 | StatusListed |
Official records
- AccessGUDID record 04057217005829
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Probe Navigator
- Generic name
- Invasive vascular ultrasound system probe
- Model / reference
- C02 500
- Primary DI / UDI-DI
- 04057217005829
- FDA product code
- LRP
- GMDN term
- Invasive vascular ultrasound system probe
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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