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LBC SD Testmate-2390 G

EUDAMED

Class A (EU MDR)

Ref 200 tests/box : CP.001.930Model 200 tests/box

by Guangzhou LBP Medicine Science & Technology Co., Ltd.

Identity

Device Name
LBC SD Testmate-2390 G EUDAMED
Model / Reference
200 tests/box EUDAMED
200 tests/box : CP.001.930 EUDAMED

Identifiers

Primary DI / UDI-DI
06948500937607 EUDAMED
Basic UDI-DI
69485009LBP014MV EUDAMED
EMDN Code
W0599 IVD GENERAL USE CONSUMABLE DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

Yes

EUDAMED

LBC SD Testmate-2390 G by Guangzhou LBP Medicine Science & Technology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000026786
Authorised Representative
Kingsmead Service B.V. NL-AR-000002066

Sources (1)

  • EUDAMED 45e9ef6d-4b7d-46fb-a269-218c4a3b4d0d 61 fields · synced Oct 6, 2026