Data from EUDAMED, last updated May 23, 2026

Aura Wash 1

4250380NEQ8

2 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: ZytoVision GmbH

Device family identification

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Status: On the market

ReagentProfessional testing

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

Data from EUDAMED, last updated May 23, 2026

4250380NEQ8

2 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: ZytoVision GmbH

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Status: On the market

ReagentProfessional testing

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

2 references

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
NOA-602	`NOA-602`	`04250380309750`	1	On the market
NOA-601	`NOA-601`	`04250380309743`	1	On the market