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SealingPro

EUDAMED

Class IIa (EU MDR)

Ref 18821100

by APT Medical Inc.

Identity

Trade Name
SealingPro EUDAMED
Device Name
SealingPro™ Y Connector EUDAMED
Model / Reference
18821100 EUDAMED

Identifiers

Primary DI / UDI-DI
06949450407189 EUDAMED
Basic UDI-DI
69494504RYC1801YK EUDAMED
EMDN Code
C01040180 CORONARY ANGIOGRAPHY DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Cyprus 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

SealingPro 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 90e95544-e19c-4cc1-89c7-27eebf9d98a4 61 fields · synced Jun 17, 2026