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Kiilto Pro MD Des IPA 45+ 5000 ml

EUDAMED

Class IIa (EU MDR)

Ref 669-3

by KiiltoClean Oy

Identity

Trade Name
Kiilto Pro MD Des IPA 45+ 5000 ml EUDAMED
Device Name
Kiilto Pro MD Des IPA 45+ EUDAMED
Model / Reference
669-3 EUDAMED

Identifiers

Primary DI / UDI-DI
07331964006696 EUDAMED
Basic UDI-DI
6417964MDL0006210A93 EUDAMED
EMDN Code
D0702 ISOPROPYL ALCOHOL FOR THE DISINFECTION OF MEDICAL DEVICES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Sweden 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 MD Des IPA 45+ 5000 ml by KiiltoClean Oy — 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
KiiltoClean Oy
EUDAMED SRN
FI-MF-000001622

Sources (1)

  • EUDAMED a4170016-18e7-445c-b50f-204b4b5a3da5 61 fields · synced Oct 7, 2026