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Fortel® Ulcer (H. pylori) Screening Test

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref 1005-1

by Biomerica, Inc.

Identity

Trade Name
Fortel® Ulcer (H. pylori) Screening Test EUDAMED
Device Name
Fortel Ulcer (H. pylori) Screening Test EUDAMED
Model / Reference
1005-1 EUDAMED

Identifiers

Primary DI / UDI-DI
00083059100518 EUDAMED
Basic UDI-DI
B-00083059100518 EUDAMED
EMDN Code
W0105090102 H. PYLORI - RT & POC EUDAMED

Classification

Device Class
Class IVD devices for self-testing EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

Yes

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Fortel® Ulcer (H. pylori) Screening Test by Biomerica, Inc. — Class IVD devices for self-testing — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
Biomerica, Inc.
EUDAMED SRN
US-MF-000015772
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED a685120a-b0dc-4f81-9a82-0ff0c9bee925 61 fields · synced Jun 18, 2026