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DrDrys

by Microcopy, A Division of Neo-Flo, Inc.

Ref DRDRYL

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081896302DRDRYD7 Basic UDI-DIDate28 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Saliva Absorbents - Non Sterile
Model / Reference
DRDRYL
Primary DI / UDI-DI
00818963020078
Basic UDI-DI
081896302DRDRYD7
EMDN Code
Q019001 Saliva aspirators and saliva absorbents
Device Class
Class I
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
US-MF-000012637
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Microcopy, A Division of Neo-Flo, Inc.

See all devices from Microcopy, A Division of Neo-Flo, Inc. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No