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Extubation Advisor v1.4.7.86

EUDAMED

Class IIb (EU MDR)

Ref 011-1000

by OBS Medical Ltd

Identity

Trade Name
Extubation Advisor v1.4.7.86 EUDAMED
Device Name
Extubation Advisor EUDAMED
Model / Reference
011-1000 EUDAMED

Identifiers

Primary DI / UDI-DI
5060457930201 EUDAMED
Basic UDI-DI
B-5060457930201 EUDAMED
EMDN Code
Z1203010592 PULMONARY VENTILATORS FOR HOSPITAL USE - MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Special Device Type
-1192 EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Extubation Advisor v1.4.7.86 by OBS Medical Ltd — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
OBS Medical Ltd
EUDAMED SRN
GB-MF-000028311
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED 39c59291-7d28-4ae6-97f6-a8ab6e65f6ea 61 fields · synced Jul 23, 2026