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Telic S.A.

by Paramount Surgimed Limited India EUDAMED

Ref DCS30Model 2.0, 3.0, 4.0, 5.0, 7.0 mm

EMDN A01020303

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8903175PSLDC65 Basic UDI-DIDate26 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Dermal Curette
Model / Reference
2.0, 3.0, 4.0, 5.0, 7.0 mm, DCS30
Primary DI / UDI-DI
28427734038158
Basic UDI-DI
8903175PSLDC65
EMDN Code
A01020303 Cutaneous biopsy curettes, single-use
Device Class
Class IIa
Market of Registration
Spain

Manufacturer details

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

Other devices from Paramount Surgimed Limited

See all devices from Paramount Surgimed Limited →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 28427734038158|8903175PSLDC65 61 fields · synced 24 Oct 2026