Data from EUDAMED, last updated Jun 11, 2026

Leishmaniasis IgG/IgM Rapid Test (Serum/Plasma)

B-697424646LEI002GZVF

1 reference

IVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Manufacturer: SAFECARE BIOTECH (HANGZHOU) CO., LTD.

Device family identification

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Status: On the market

ReagentProfessional testingAnimal tissues / cells

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

References

1 reference

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Leishmaniasis IgG/IgM Rapid Test (Serum/Plasma)	`LEI-3021/LEI-3022`	`D-697424646LEI002GZVF`	1	On the market