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Single-use Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref BFTW-1629E-YGModel BFUW-1029P-YG、 BFTW-1629E-YG、BFUW-1629E-YG、BFTW-1829E-YG、 BFTN-1829E-YG、BFUW-1829E-YG、BFUN-1829E-YG

by Scivita Medical Technology Co., Ltd.

Identity

Trade Name
Single-use Biopsy Forceps EUDAMED
Device Name
Single-use Biopsy Forceps EUDAMED
Model / Reference
BFUW-1029P-YG、 BFTW-1629E-YG、BFUW-1629E-YG、BFTW-1829E-YG、 BFTN-1829E-YG、BFUW-1829E-YG、BFUN-1829E-YG EUDAMED
BFTW-1629E-YG EUDAMED

Identifiers

Primary DI / UDI-DI
06971381258103 EUDAMED
Basic UDI-DI
697138125036A8V EUDAMED
Direct Marketing DI
06971381258103 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Single-use Biopsy Forceps by Scivita 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

Manufacturer
Scivita Medical Technology Co., Ltd.
EUDAMED SRN
CN-MF-000010305
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED d3e6dd5f-58b6-417a-ab1c-f87e9ca3409a 61 fields · synced May 29, 2026