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Stimulating Dissection Instrument

by Beckdal (Shanghai) MedTech Co., Ltd. 10 variants

Ref 1060000700Model SI100014

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-06974884200631 Basic UDI-DI 06974884200631UDI-DIDate27 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  • Withdrawn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
SI100014, 1060000700
Primary DI / UDI-DI
06974884200631
Basic UDI-DI
B-06974884200631
EMDN Code
N010180 Neurophysiology devices - accessories
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CN-MF-000042207
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Beckdal (Shanghai) MedTech Co., Ltd.

See all devices from Beckdal (Shanghai) MedTech Co., Ltd. →

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