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Sereny™ Hemostasis Introducer

EUDAMED

Class IIa (EU MDR)

Ref 152C061535Model 4F, 5F, 6F, 7F, 8F

by APT Medical Inc.

Identity

Trade Name
Sereny™ Hemostasis Introducer EUDAMED
Device Name
Sereny™ Hemostasis Introducer EUDAMED
Model / Reference
4F, 5F, 6F, 7F, 8F EUDAMED
152C061535 EUDAMED

Identifiers

Primary DI / UDI-DI
06942075353299 EUDAMED
Basic UDI-DI
69318961INS152SE EUDAMED
EMDN Code
C0502 CARDIOVASCULAR INTRODUCER SHEATHS, VALVED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Vascular catheter introduction set, nonimplantable

Sereny™ Hemostasis Introducer by APT Medical Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

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 abaab9a8-5c4d-455e-b686-08d0d3da1bab 61 fields · synced Aug 1, 2026