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Pharma Lab

EUDAMED

Class IIa (EU MDR)

Ref CURET-7Model 2.0, 3.0, 4.0, 5.0, 7.0 mm

by Paramount Surgimed Limited

Identity

Trade Name
PHARMA LAB EUDAMED
Device Name
Dermal Curette EUDAMED
Model / Reference
2.0, 3.0, 4.0, 5.0, 7.0 mm EUDAMED
CURET-7 EUDAMED

Identifiers

Primary DI / UDI-DI
03615370004656 EUDAMED
Basic UDI-DI
8903175PSLDC65 EUDAMED
EMDN Code
A01020303 CUTANEOUS BIOPSY CURETTES, 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: Dermal curette, single-use

Pharma Lab by Paramount Surgimed Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dermal curette, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000021682
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 73db6876-50be-4f48-a997-d815e90f11f8 61 fields · synced Jul 22, 2026