Data from EUDAMED, last updated Jun 11, 2026

2019-nCoV Antigen Rapid Test Cassette Nasopharyngeal and Oropharyngeal Swab

B-06974323017271

1 reference

IVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Manufacturer: Beijing Applied Biological Technologies Co., Ltd.

Device family identification

Device name: 2019-nCoV Antigen Rapid Test Cassette Nasopharyngeal and Oropharyngeal Swab
Basic UDI-DI: B-06974323017271
Issuing agency: EUDAMED
Version date: May 13, 2026

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

ReagentProfessional testing

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
IH003	`IH003`	`06974323017271`	1	On the market