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Benefis

EUDAMED

Class IIa (EU MDR)

Ref B010133 Soft 33G

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
Benefis EUDAMED
Device Name
Disposable Blood Lancets EUDAMED
Model / Reference
B010133 Soft 33G EUDAMED

Identifiers

Primary DI / UDI-DI
06945630135699 EUDAMED
Basic UDI-DI
6945630101B9 EUDAMED
Unit of Use DI
16945630135696 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Benefis by Sterilance Medical (Suzhou) Inc. — Class IIa — 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-000002860
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED caf12dca-27a4-41c3-b653-d9b018c64d31 61 fields · synced Jun 18, 2026