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Aptē

EUDAMED

Class IIb (EU MDR)

Ref SKA30040Model APS

by Adria Med S.r.l.

Identity

Trade Name
APTĒ EUDAMED
Device Name
APTĒ EUDAMED
Model / Reference
APS EUDAMED
SKA30040 EUDAMED

Identifiers

Primary DI / UDI-DI
08052204714247 EUDAMED
Basic UDI-DI
80522047103SKAQR EUDAMED
EMDN Code
A05010101 ELASTOMERIC SYSTEMS - FIXED FLOW W/O ADDITIONAL BOLUS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Elastomeric infusion pump system

Aptē by Adria Med S.r.l. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Elastomeric infusion pump system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Adria Med S.r.l.
EUDAMED SRN
IT-MF-000020866

Sources (1)

  • EUDAMED d5b0caf5-4977-422c-bd42-7fe5f3d5590c 61 fields · synced Jun 17, 2026