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RTU set

by Cobes Industries(Hefei) Co., Ltd 2 variants

Part of a family of 15 devices: see the family page

Ref 406238Model General Surgical Pack

RTU set (406238) is a Class I device made by Cobes Industries(Hefei) Co., Ltd, registered in EUDAMED on 16 Mar 2024 (Basic UDI-DI 69562886MA0002LC), 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 Number69562886MA0002LC Basic UDI-DI 06956288674126UDI-DIDate16 Mar 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
General Surgical Pack
Model / reference
General Surgical Pack, 406238
Primary DI / UDI-DI
06956288674126
Basic UDI-DI
69562886MA0002LC
EMDN code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000012364
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

Other devices filed under SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS).

Other devices from Cobes Industries(Hefei) Co., Ltd

See all devices from Cobes Industries(Hefei) Co., Ltd →

Properties

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