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Medical plastic forceps

EUDAMED

Class I (EU MDR)

Ref SP-PDFBModel Is

by Shaoxing Yibon Medical Co., Ltd.

Identity

Trade Name
Medical plastic forceps EUDAMED
Device Name
Medical plastic forceps EUDAMED
Model / Reference
Is EUDAMED
SP-PDFB EUDAMED

Identifiers

Primary DI / UDI-DI
06972370761543 EUDAMED
Basic UDI-DI
697237076YB1ST04V4 EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED

Classification

Device Class
Class I 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: Surgical retractor/retraction system blade, single-use

Medical plastic forceps by Shaoxing Yibon Medical Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, 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-000003378
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 11b9c815-7d6b-49c5-adee-4b799c34a3d7 61 fields · synced Jun 19, 2026