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Kiilto Pro Erisan Des 3 l

EUDAMED

Class IIa (EU MDR)

Ref 8127

by KiiltoClean Oy

Identity

Trade Name
Kiilto Pro Erisan Des 3 l EUDAMED
Device Name
Kiilto Pro Erisan Des EUDAMED
Kiilto Pro Erisan Des 3 l EUDAMED
Model / Reference
8127 EUDAMED

Identifiers

Primary DI / UDI-DI
06417964081275 EUDAMED
Basic UDI-DI
6417964MDL031013808U EUDAMED
B-06417964081275 EUDAMED
EMDN Code
D0902 ASSOCIATED AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland 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

Kiilto Pro Erisan Des 3 l by KiiltoClean Oy — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
KiiltoClean Oy
EUDAMED SRN
FI-MF-000001622

Sources (2)

  • EUDAMED bd24f809-8443-489a-ad70-0c7cdfbb2702 61 fields · synced Oct 6, 2026
  • EUDAMED bec42f6b-9578-455d-b61b-5f8bf19e6fc7 61 fields · synced May 19, 2026