Data from EUDAMED, last updated Jun 11, 2026

Mycoplasma pneumoniae(MP) IgG/IgM Combo Rapid Test(Serum/Plasma)

B-697424646MP002HKLS

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

Device name: Mycoplasma pneumoniae(MP) IgG/IgM Combo Rapid Test(Serum/Plasma)
Basic UDI-DI: B-697424646MP002HKLS
Issuing agency: EUDAMED
Version date: May 19, 2026

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
Mycoplasma pneumoniae(MP) IgG/IgM Combo Rapid Test(Serum/Plasma)	`MP-3021/MP-3022`	`D-697424646MP002HKLS`	1	On the market