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KangLi

by Suzhou Kangli Orthopaedics Instrument Co., Ltd. 1,000+ variants

Ref T5877050Model Non-sterile Spinal Systems(KSS-II, III Lumbar)

KangLi (T5877050) is a Class IIb device made by Suzhou Kangli Orthopaedics Instrument Co., Ltd., registered in EUDAMED on 25 Aug 2023 (Basic UDI-DI 690295900030FD), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number690295900030FD Basic UDI-DI 06937762120360UDI-DIDate25 Aug 2023RegisteredStatusActive EUDAMED: not on the EU market

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Non-sterile Spinal Systems
Model / reference
Non-sterile Spinal Systems(KSS-II, III Lumbar), T5877050
Primary DI / UDI-DI
06937762120360
Basic UDI-DI
690295900030FD
Direct marketing DI
06937762120360
EMDN code
P09070302 Thoracolumbosacral fixation systems
Device class
Class IIb
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
CN-MF-000016075
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Related devices

Category: Spinal bone screw, non-bioabsorbable

Similar devices in this category

Other devices filed under THORACOLUMBOSACRAL FIXATION SYSTEMS.

Other devices from Suzhou Kangli Orthopaedics Instrument Co., Ltd.

Properties

  • Sterilise before use
  • Implantable
  • Reprocessed single-use device
  • Sutures
Other properties (11, all answered No)