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Selepump®

EUDAMED

Class I (EU MDR)

Ref K-P-40

by Kossel Medtech (Suzhou) Co., Ltd.

Identity

Trade Name
SELEPUMP® EUDAMED
Device Name
Inflation Device EUDAMED
Model / Reference
K-P-40 EUDAMED

Identifiers

Primary DI / UDI-DI
06971591763558 EUDAMED
Basic UDI-DI
697159176INFLATION5F EUDAMED
EMDN Code
C0699 CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I 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

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

Category: Surgical bulldog clamp, single-use

Selepump® by Kossel Medtech (suzhou) Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000012352
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED d94a5d55-00ab-480e-9068-bb181a815437 61 fields · synced Jul 11, 2026