← Back to catalogue

upper Roots Forceps

EUDAMED

Class I (EU MDR)

Ref 523

by Prilanta Surgical

Identity

Device Name
upper Roots Forceps EUDAMED
Model / Reference
523 EUDAMED

Identifiers

Primary DI / UDI-DI
G5485230 EUDAMED
Basic UDI-DI
++G548523N7 EUDAMED
EMDN Code
L03130402 FORCEPS FOR EXTERNAL BODIES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Bronchoscopic biopsy curette, rigid

upper Roots Forceps by Prilanta Surgical — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bronchoscopic biopsy curette, rigid.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Prilanta Surgical
EUDAMED SRN
PK-MF-000038228
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED da19d2d4-a336-406d-aa8c-89accebe22fd 61 fields · synced Jul 9, 2026