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Hanarostent®

EUDAMED

Class IIb (EU MDR)

Ref HRC-20-080-230Model HANAROSTENT® Intestine Asymmetric (NCN)

by M.I.Tech Co., Ltd

Identity

Trade Name
HANAROSTENT® EUDAMED
Device Name
Colon/Rectum Stent with Delivery System EUDAMED
Model / Reference
HANAROSTENT® Intestine Asymmetric (NCN) EUDAMED
HRC-20-080-230 EUDAMED

Identifiers

Primary DI / UDI-DI
08806367024893 EUDAMED
Basic UDI-DI
B-08806367024893 EUDAMED
EMDN Code
P0503 COLONIC AND DUODENAL PROSTHESES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Hanarostent® by M.I.Tech Co., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
M.I.Tech Co., Ltd
EUDAMED SRN
KR-MF-000011623
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED 976ae525-848b-4216-ae5e-8cbe1de4f832 61 fields · synced May 23, 2026