← Back to catalogue

Alsevers F

EUDAMED

Class A (EU MDR)

Ref 806506Ref 806505

by Bio-Rad Medical Diagnostics GmbH

Identity

Trade Name
Alsevers F EUDAMED
Device Name
Alsevers F EUDAMED
Model / Reference
806506 EUDAMED
806505 EUDAMED

Identifiers

Primary DI / UDI-DI
07611969951345 EUDAMED
07611969951338 EUDAMED
Basic UDI-DI
361052A002918A EUDAMED
EMDN Code
W010399 HAEMATOLOGY / HAEMOSTASIS / IMMUNOHAEMATOLOGY / HISTOLOGY / CYTOLOGY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Alsevers F by Bio-Rad Medical Diagnostics Gmbh — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000019864

Sources (2)

  • EUDAMED a859dac6-edcc-4539-bc89-c5f9754e46c0 61 fields · synced Aug 1, 2026
  • EUDAMED 3bf1b9ff-c889-43f5-8a8a-1c053b108293 61 fields · synced May 19, 2026