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Respiratory Humidifier

EUDAMED

Class IIb (EU MDR)

Ref 7100008Model InterActive

by Intersurgical Ltd

Identity

Device Name
Respiratory Humidifier EUDAMED
Model / Reference
InterActive EUDAMED
7100008 EUDAMED

Identifiers

Primary DI / UDI-DI
05030267163878 EUDAMED
Basic UDI-DI
05030267HUMBASEBF EUDAMED
Direct Marketing DI
05030267163878 EUDAMED
EMDN Code
R060201 ACTIVE VENTILATION HUMIDIFICATION SYSTEMS, EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain 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

Respiratory Humidifier by Intersurgical Ltd — Class IIb — 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
Intersurgical Ltd
EUDAMED SRN
GB-MF-000004798
Authorised Representative
UAB Intersurgical LT-AR-000003907

Sources (1)

  • EUDAMED 89f19fb6-2013-4c74-9b5c-14ef27945025 61 fields · synced Jul 17, 2026