Data from EUDAMED, last updated Jun 11, 2026

Multi-Respiratory Virus Antigen Test(Swab) (Influenza A+B/ COVID-19)

B-697424646FCO000PKX7H

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: Multi-Respiratory Virus Antigen Test(Swab) (Influenza A+B/ COVID-19)
Basic UDI-DI: B-697424646FCO000PKX7H
Issuing agency: EUDAMED
Version date: May 21, 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
Multi-Respiratory Virus Antigen Test(Swab) (Influenza A+B/ COVID-19)	`FCO-6032a/FCO-6032b`	`D-697424646FCO000PKX7H`	1	On the market