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Negatoscopio 2/P Blanco

EUDAMED

Class I (EU MDR)

Ref 6002.MModel NEGATOSCOPIO

by Fabricados Triton, S.L.

Identity

Trade Name
NEGATOSCOPIO 2/P BLANCO EUDAMED
Device Name
NEGATOSCOPIO EUDAMED
Model / Reference
NEGATOSCOPIO EUDAMED
6002.M EUDAMED

Identifiers

Primary DI / UDI-DI
8424591600203 EUDAMED
Basic UDI-DI
8424591NGVH EUDAMED
Direct Marketing DI
8424591600203 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Device sterilization/disinfection container, reusable

Negatoscopio 2/P Blanco by Fabricados Triton, S.L. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/MDR

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Manufacturer

EUDAMED SRN
ES-MF-000018967

Sources (1)

  • EUDAMED a9d5a70a-4f47-4980-a898-08799a124e2f 61 fields · synced Jun 17, 2026