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Lcrb-N76m01-Oh058

EUDAMED

Class I (EU MDR)

Ref LCRB-N76M01-OH058Model Universal Pack、Universal Pack-I、Universal Pack-II、Universal Pack-III、Universal Pack-IV、Universal Pack-V、Universal Pack-VI

by Leboo Healthcare Products Limited

Identity

Model / Reference
Universal Pack、Universal Pack-I、Universal Pack-II、Universal Pack-III、Universal Pack-IV、Universal Pack-V、Universal Pack-VI EUDAMED
LCRB-N76M01-OH058 EUDAMED

Identifiers

Primary DI / UDI-DI
06974424840594 EUDAMED
Basic UDI-DI
697442484L33QL 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

Lcrb-N76m01-Oh058 by Leboo 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-000008521
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 9c8ab01e-6229-4d99-a1ac-8d550ad47986 61 fields · synced Oct 9, 2026