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Power-Endo

EUDAMED

Class IIa (EU MDR)

Ref ENDO-BF1-18-120-O1Model ENDO-BF

by Jiangsu Power-endo Medical Technology Co., Ltd

Identity

Trade Name
POWER-ENDO EUDAMED
Device Name
Disposable biopsy forceps EUDAMED
Model / Reference
ENDO-BF EUDAMED
ENDO-BF1-18-120-O1 EUDAMED

Identifiers

Primary DI / UDI-DI
06975597850632 EUDAMED
Basic UDI-DI
697559785PE04UA EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Category: Flexible endoscopic biopsy forceps, single-use

Power-Endo by Jiangsu Power-endo Medical Technology Co., Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000030213
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 9c43e593-4d8a-432d-b6eb-d376ed713dc1 61 fields · synced Jun 19, 2026