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Fortel Ultra Sensitive Pregnancy Midstream 1-Test

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref 1147-01

by Biomerica, Inc.

Identity

Trade Name
Fortel Ultra Sensitive Pregnancy Midstream 1-Test EUDAMED
Device Name
Fortel Ultra Sensitive Pregnancy Midstream 1-Test EUDAMED
Model / Reference
1147-01 EUDAMED

Identifiers

Primary DI / UDI-DI
00083059114713 EUDAMED
Basic UDI-DI
B-00083059114713 EUDAMED
EMDN Code
W0102160302 HCG - 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 Ultra Sensitive Pregnancy Midstream 1-Test by Biomerica, Inc. — Class IVD devices for self-testing — IVDD — listed in EUDAMED

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 4608fe25-0ab5-4dcf-b6f7-7de6a8a2fb1d 61 fields · synced Oct 6, 2026