Data from EUDAMED, last updated May 23, 2026

IRMA ACTH

150995905ACTHIRMAYL

2 references

IVDR Class C

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class C
Manufacturer: IMMUNOTECH s.r.o.

Device family identification

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

150995905ACTHIRMAYL

2 references

IVDR Class C

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class C
Manufacturer: IMMUNOTECH s.r.o.

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class C
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
IM2030	`IM2030`	`15099590216429`	1	On the market
B89463	`B89463`	`15099590680046`	1	On the market