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RTP® Pathogen Kit (250)

EUDAMED

Class A (EU MDR)

Ref 1040500300

by ALS Life Sciences Portugal, S.A.

Identity

Trade Name
RTP® Pathogen Kit (250) EUDAMED
Device Name
RTP® Pathogen Kit EUDAMED
Model / Reference
1040500300 EUDAMED

Identifiers

Primary DI / UDI-DI
05600236235136 EUDAMED
Basic UDI-DI
5600236235AA013E8 EUDAMED
EMDN Code
W0105900101 REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

Category: Nucleic acid extraction/isolation kit IVD

RTP® Pathogen Kit (250) by ALS Life Sciences Portugal, S.A. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
PT-MF-000034751

Sources (1)

  • EUDAMED a218ffb4-dec1-4801-8419-e399f4c0f4e8 61 fields · synced Jul 18, 2026