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PCF Rod

by Shandong Weigao Orthopaedic Device Company Limited. 12 variants

Part of a family of 21 devices: see the family page

Ref 800002030Model WGB1Z-4, WGB1Z-7-04

PCF Rod (800002030) is a Class IIb device made by Shandong Weigao Orthopaedic Device Company Limited., registered in EUDAMED on 27 Nov 2025 (Basic UDI-DI 6903095SPIWGB1Z4RD64), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6903095SPIWGB1Z4RD64 Basic UDI-DI 06939488337510UDI-DIDate27 Nov 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Sterile and Non Sterile Spinal System
Model / reference
WGB1Z-4, 800002030, WGB1Z-7-04
Primary DI / UDI-DI
06939488337510
Basic UDI-DI
6903095SPIWGB1Z4RD64, 6903095SPIWGB1Z704PRUU
EMDN code
P09070301 Cervical fixation systems
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Lithuania
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000019785
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Similar devices in this category

Other devices filed under CERVICAL FIXATION SYSTEMS.

Other devices from Shandong Weigao Orthopaedic Device Company Limited.

See all devices from Shandong Weigao Orthopaedic Device Company Limited. →

Properties

  • Sterilise before use
  • Implantable
  • Sutures
Other properties (12, all answered No)