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Container, Sterilisation

by Geister Medizintechnik GmbH 725 variants

Part of a family of 732 devices: see the family page

Ref 77-0103.PE

Container, Sterilisation (77-0103.PE) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 405703400000001ZP), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number405703400000001ZP Basic UDI-DI 04057034301302UDI-DIDate8 Oct 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Container, Sterilisation
Model / reference
77-0103.PE
Primary DI / UDI-DI
04057034301302
Basic UDI-DI
405703400000001ZP
Direct marketing DI
04057034301302
EMDN code
S010402 Filters for sterilisation containers
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005461

Similar devices in this category

Other devices filed under CONTAINERS FOR STERILISATION.

Other devices from Geister Medizintechnik GmbH

See all devices from Geister Medizintechnik GmbH →

Properties

  • Sterilise before use
Other properties (13, all answered No)