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Sterilisationscontainer

by REDA Instrumente GmbH 846 variants

Ref R 310.20

Sterilisationscontainer (R 310.20) is a Class I device made by REDA Instrumente GmbH, registered in EUDAMED on 27 May 2026 (Basic UDI-DI 4063058000001964F), 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 Number4063058000001964F Basic UDI-DI 04063058063980UDI-DIDate27 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Sterilisationscontainer
Model / reference
R 310.20
Primary DI / UDI-DI
04063058063980
Basic UDI-DI
4063058000001964F
Direct marketing DI
04063058063980
EMDN code
V0499 Clinical use containers (non-IVD) - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005592

Related devices

Category: Instrument transport trolley system

Other devices from REDA Instrumente GmbH

See all devices from REDA Instrumente GmbH →

Properties

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