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PrintoSept-ID

EUDAMED

Class IIa (EU MDR)

Ref 4500

by Alpro Medical Gmbh

Identity

Trade Name
PrintoSept-ID EUDAMED
Device Name
PrintoSept-ID EUDAMED
Model / Reference
4500 EUDAMED

Identifiers

Primary DI / UDI-DI
+E25145001 EUDAMED
Basic UDI-DI
++E251006060009H EUDAMED
Direct Marketing DI
+E25145001 EUDAMED
EMDN Code
D99 DISINFECTANTS, ANTISEPTICS, STERILISING AGENTS AND DETERGENTS FOR MEDICAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

PrintoSept-ID by Alpro Medical Gmbh — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Alpro Medical Gmbh
EUDAMED SRN
DE-MF-000010603

Sources (1)

  • EUDAMED b794385a-9549-4d32-b67d-2d14104d28ac 61 fields · synced Oct 6, 2026