← Back to catalogue

Humidose

EUDAMED

Class I (EU MDR)

Ref 112170

by Orion Oyj

Identity

Trade Name
Humidose EUDAMED
Nasolin Humidose EUDAMED
Device Name
Humidose EUDAMED
Nasolin Humidose EUDAMED
Model / Reference
112170 EUDAMED

Identifiers

Primary DI / UDI-DI
06432100001023 EUDAMED
Basic UDI-DI
B-06432100001023 EUDAMED
643210HUM001VT EUDAMED
EMDN Code
Q030103 NASAL IRRIGATION SOLUTIONS EUDAMED

Classification

Device Class
Class I EUDAMED
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

Humidose by Orion Oyj — Class I — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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

Manufacturer

Manufacturer
Orion Oyj
EUDAMED SRN
FI-MF-000001595

Sources (2)

  • EUDAMED 073fcb0b-bcfa-456f-ade8-cee79ea73a58 61 fields · synced Aug 3, 2026
  • EUDAMED dd2845d9-d69a-4c4a-8071-c1d403967db1 61 fields · synced May 18, 2026