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Hemorrhoidectomy Pack

EUDAMED

Class I (EU MDR)

Ref N76D03-OH002Model N76D03 O76D03 N76D03-00 N76D03-01 N76D03-02 N76D03-03

by Leboo (Hubei) Healthcare Products Limited

Identity

Device Name
Hemorrhoidectomy Pack EUDAMED
Model / Reference
N76D03 O76D03 N76D03-00 N76D03-01 N76D03-02 N76D03-03 EUDAMED
N76D03-OH002 EUDAMED

Identifiers

Primary DI / UDI-DI
06975197846103 EUDAMED
Basic UDI-DI
697519784Z61WT EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Hemorrhoidectomy Pack by Leboo (Hubei) Healthcare Products Limited — Class I — 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

EUDAMED SRN
CN-MF-000021186
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED 7eb41d1c-903d-4127-960d-c361b67b9569 61 fields · synced Oct 6, 2026