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Benefis

EUDAMED

Class IIa (EU MDR)

Ref BM22

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
Benefis EUDAMED
Device Name
Disposable Scalpels EUDAMED
Model / Reference
BM22 EUDAMED

Identifiers

Primary DI / UDI-DI
16945630123846 EUDAMED
Basic UDI-DI
6945630107BM EUDAMED
Unit of Use DI
06945630123849 EUDAMED
EMDN Code
V010101 SCALPELS WITH 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 00dd8098-560d-4e4d-81bc-80574dc3f05b 61 fields · synced Jun 19, 2026