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Shoocin™

by Lepu Medical Technology (Beijing) Co., Ltd. 1,000+ variants

Part of a family of 30 devices: see the family page

Ref RS042421Model RS series, no guidewire

Shoocin™ (RS042421) is a Class IIa device made by Lepu Medical Technology (Beijing) Co., Ltd., registered in EUDAMED on 9 May 2026 (Basic UDI-DI 69367337LP0026MQ), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69367337LP0026MQ Basic UDI-DI 06936733776285UDI-DIDate9 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Introducer Kit
Model / reference
RS series, no guidewire, RS042421
Primary DI / UDI-DI
06936733776285
Basic UDI-DI
69367337LP0026MQ
EMDN code
C01040280 Peripheral angiography devices - accessories not included in other classes
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Cyprus

Manufacturer details

EUDAMED SRN
CN-MF-000001408
Authorised representative
Lepu Medical (Europe) Cooperatief U.A. NL-AR-000000551

Similar devices in this category

Other devices filed under PERIPHERAL ANGIOGRAPHY DEVICES.

Other devices from Lepu Medical Technology (Beijing) Co., Ltd.

See all devices from Lepu Medical Technology (Beijing) Co., Ltd. →

Properties

  • Supplied sterile
Other properties (13, all answered No)