← Back to catalogue

Dentosept® S

EUDAMED

Class IIa (EU MDR)

Ref 6603273

by Alpro Medical Gmbh

Identity

Trade Name
Dentosept® S EUDAMED
Device Name
Dentosept® EUDAMED
Model / Reference
6603273 EUDAMED

Identifiers

Primary DI / UDI-DI
+E25166032731 EUDAMED
Basic UDI-DI
++E251001026007J EUDAMED
Direct Marketing DI
+E25166032731 EUDAMED
EMDN Code
D0599 OXYGEN PRODUCERS FOR DISINFECTION OF 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

Dentosept® S 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Alpro Medical Gmbh
EUDAMED SRN
DE-MF-000010603

Sources (1)

  • EUDAMED 62a1f024-f21d-460b-b4be-df7f7f22210e 61 fields · synced Oct 6, 2026