Data from EUDAMED, last updated May 30, 2026

DIAWHITE 50

8033895W01030799Diawh50E6

3 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: Diapath S.p.A. società a socio unico

Device family identification

Device name: DIAWHITE 50
Basic UDI-DI: 8033895W01030799Diawh50E6
Device model: ALCOHOLIC COLOURLESS MIXTURE, ALCOHOLIC DEGREE 50 - DIAWHITE 50
Issuing agency: GS1
Version date: May 11, 2026

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.

References

3 references

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
DONATELLO SERIES TANK_DIAWHITE 50 - 5 LT	`N0255`	`08033895009768`	1	On the market
DONATELLO TANK_DIAWHITE 50 - 4.1 LT	`H0255`	`08033895009539`	1	On the market
DONATELLO TANK_DIAWHITE 50 NO RFID 4.1 LT	`H0255WR`	`08033895009546`	1	On the market