Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “Eight Respiratory Pathogen Antigen Rapid Test Kit (LFIA)”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 6 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 6

More countries (2)

Finland 4 Poland 2

Risk class Class I Class IIa Class IIb Class III Class II (US)

More classes (11)

Class A Class B Class C 6 Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

Verified Verified only

Category (EMDN)

Browse by category

6 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

H&W Eight Respiratory Pathogen Antigen Rapid Test Kit (LFIA)

Jiangsu Medomics Medical Technology Co., Ltd.,China

Active Regimes: CE IVDR Registry: EUDAMED Class:C
Eight Respiratory Pathogen Antigen Rapid Test Kit (LFIA)

Jiangsu Medomics Medical Technology Co., Ltd.,China Group of variants

Active Regimes: CE IVDR Registry: EUDAMED Class:C

Previous Next

Showing 1-6 of 6

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site