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Aesthesio

by Danmic Global, LLC 9 variants

Part of a family of 9 devices: see the family page

Ref 514000-20C

Aesthesio (514000-20C) is a Class I device made by Danmic Global, LLC, registered in EUDAMED on 20 Jan 2026 (Basic UDI-DI 0850006095Aesthesio5R), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0850006095Aesthesio5R Basic UDI-DI 00850006095162UDI-DIDate20 Jan 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  • Withdrawn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

Model / reference
514000-20C
Primary DI / UDI-DI
00850006095162
Basic UDI-DI
0850006095Aesthesio5R
Direct marketing DI
00850006095162
EMDN code
V9099 Various devices not included in other classes - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
US-MF-000021060
Authorised representative
Code of Practice AB SE-AR-000003002

Related devices

Category: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Danmic Global, LLC

See all devices from Danmic Global, LLC →

Properties

Other properties (14, all answered No)