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Straight Bipolar Forceps, 0.5 mm Tip, 6" or 15.2 cm, 3M Cable, European Pattern, Single Use, Sterile

by The Surge International

Ref PMS5301

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-08964002861668 Basic UDI-DI 08964002861668UDI-DIDate19 May 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
PMS5301
Primary DI / UDI-DI
08964002861668
Basic UDI-DI
B-08964002861668
EMDN Code
K0201010601 Open electrosurgery forceps, single-use
Device Class
Class IIb
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
PK-MF-000043013
Authorised representative
Obelis s.a. BE-AR-000000106

From the manufacturer

Manufacturer's product page: European

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See all devices from The Surge International →

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