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OmniPump™

EUDAMED

Class IIa (EU MDR)

Ref 166S-IP-1

by APT Medical Inc.

Identity

Trade Name
OmniPump™ EUDAMED
Device Name
OmniPump™ Irrigation Tubing Set EUDAMED
Model / Reference
166S-IP-1 EUDAMED

Identifiers

Primary DI / UDI-DI
06931896185585 EUDAMED
Basic UDI-DI
69318961GZGLS166SX3 EUDAMED
EMDN Code
Z12030385 INFUSION INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

OmniPump™ by APT Medical Inc. — 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
APT Medical Inc.
EUDAMED SRN
CN-MF-000009046
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED c6541ed7-8ff0-4dea-80d0-03b615a07484 61 fields · synced Jul 9, 2026