Results for “Single-use Container for Human Venous Blood Specimen Collection”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

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

Country / market European Union (all) United States

More countries (18)

Germany Italy Türkiye France Netherlands Spain Austria Poland Belgium Ireland Czechia Portugal Greece Sweden Hungary Denmark Romania Liechtenstein

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

More classes (11)

Class A Class B Class C 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

146 devices foundsorted by relevance

Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Single-use Containers for Human Venous Blood Specimen Collection

Hebei Xinle Sci&Tech Co., Ltd.,China Group of variants

Active Regimes: CE IVDR Registry: EUDAMED Class:A

Previous Next

Showing 21-40 of 146

deviCERTS Global Medical Device Regulatory Database

About [email protected]

Results for “Single-use Container for Human Venous Blood Specimen Collection”

Category (EMDN)

Single-use Containers for Human Venous Blood Specimen Collection