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Miscellaneous

by devemed GmbH 30 variants

Ref 8300-17

Miscellaneous (8300-17) is a Class I device made by devemed GmbH, registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI 4061644PG0702020383), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4061644PG0702020383 Basic UDI-DI 04061644017775UDI-DIDate14 Jul 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  • Withdrawn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
Miscellaneous
Model / reference
8300-17
Primary DI / UDI-DI
04061644017775
Basic UDI-DI
4061644PG0702020383
Direct marketing DI
04061644017775
EMDN code
S9080 Devices for sterilisation (excluding cat. d - z) - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005568

Similar devices in this category

Other devices filed under DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - ACCESSORIES.

Other devices from devemed GmbH

See all devices from devemed GmbH →

Properties

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