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Single Use Bipolar Forceps

EUDAMED

Class IIb (EU MDR)

Ref SU-0202-1020-5

by B&H Surgical Instrument

Identity

Device Name
Single Use Bipolar Forceps EUDAMED
Model / Reference
SU-0202-1020-5 EUDAMED

Identifiers

Primary DI / UDI-DI
+B969SU020210205 EUDAMED
Basic UDI-DI
++B969SUBIPOLARFORCEPSCB EUDAMED
EMDN Code
K02010199 MONO- AND BIPOLAR INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

Single Use Bipolar Forceps by B&H Surgical Instrument — Class IIb — 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
PK-MF-000012820
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 0b55a517-1f85-43ab-8604-75416a26dd6a 61 fields · synced Jul 19, 2026