← Back to catalogue

Lb-N76m01-Os03ia-B00

EUDAMED

Class I (EU MDR)

Ref LB-N76M01-OS03IA-B00Model 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
LB-N76M01-OS03IA-B00 EUDAMED

Identifiers

Primary DI / UDI-DI
06974424848491 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

Lb-N76m01-Os03ia-B00 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000008521
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 85904687-a7bc-4550-80c7-2ebe5acd1227 61 fields · synced Jun 19, 2026