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M-Plast

by Aso LLC

Part of a family of 13 devices: see the family page

Ref BEV-9382Model 188962 / 18-3362

M-Plast (BEV-9382) is a Class I device made by Aso LLC, registered in EUDAMED on 26 Apr 2024 (Basic UDI-DI 0017276188962S4), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0017276188962S4 Basic UDI-DI 08712175944448UDI-DIDate26 Apr 2024RegisteredStatusActive

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  • Withdrawn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
Nasal Dilator Triple Bridge Tan P2S
Model / reference
188962 / 18-3362, BEV-9382
Primary DI / UDI-DI
08712175944448
Basic UDI-DI
0017276188962S4
EMDN code
M0599 Medical plasters - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000008641
Authorised representative
Aso Europe BV NL-AR-000004377

Similar devices in this category

Other devices filed under MEDICAL PLASTERS - OTHER.

Other devices from Aso LLC

See all devices from Aso LLC →

Properties

Other properties (14, all answered No)