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InviSorb® Spin Universal Kit (50)

EUDAMED

Class A (EU MDR)

Ref 1050100200

by ALS Life Sciences Portugal, S.A.

Identity

Trade Name
InviSorb® Spin Universal Kit (50) EUDAMED
Device Name
InviSorb® Spin Universal Kit EUDAMED
Model / Reference
1050100200 EUDAMED

Identifiers

Primary DI / UDI-DI
05600236235143 EUDAMED
Basic UDI-DI
5600236235AA015EC 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

InviSorb® Spin Universal Kit (50) by ALS Life Sciences Portugal, S.A. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

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 0f3654b3-08c4-4070-bddd-439a30c6f2ad 61 fields · synced Jul 13, 2026