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Nextech

by Paramount Surgimed Limited 34 variants

Ref BPS6.0 (Primary)Model Biopsy Punch- 6.0mm (size)

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08903175091618 Basic UDI-DI 08903175091618UDI-DIDate26 Oct 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Biopsy Punch
Model / Reference
Biopsy Punch- 6.0mm (size), BPS6.0 (Primary)
Primary DI / UDI-DI
08903175091618
Basic UDI-DI
B-08903175091618
EMDN Code
A01020302 Cutaneous biopsy punches, single-use
Device Class
Class IIa
EU market of registration
France

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

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No