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Medical Oil-free Air Compressor

by Suzhou Pelement Medical Technology Co., Ltd. 7 variants

Ref A101、A102、A103、A104、A105、A201、A202、A203、A204、A205、A301、A302、A303、A304、A305、A401、A402、A403、A404、A406、A408、A410, A101、A102、A103、A104、A105、A201、A202、A203、A204、A205、A301Model A101、A102、A103、A104、A105、A201、A202、A203、A204、A205、A301、A302、A303、A304、A305、A401、A402、A403、A404、A406、A408、A410、A501、A502、A503、A504、A506、A508、A510、A701、A702、A703、A704、A705

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697776405363F Basic UDI-DI Date16 Oct 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
A101、A102、A103、A104、A105、A201、A202、A203、A204、A205、A301、A302、A303、A304、A305、A401、A402、A403、A404、A406、A408、A410、A501、A502、A503、A504、A506、A508、A510、A701、A702、A703、A704、A705, A101、A102、A103、A104、A105、A201、A202、A203、A204、A205、A301、A302、A303、A304、A305、A401、A402、A403、A404、A406、A408、A410, A101、A102、A103、A104、A105、A201、A202、A203、A204、A205、A301
Primary DI / UDI-DI
06977764050043, 06977764050029
Basic UDI-DI
697776405363F, 6977764022GH
Direct Marketing DI
06977764050043
06977764050029
EMDN Code
Q019001 Saliva aspirators and saliva absorbents
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000044569
Authorised representative
REP Europe GmbH DE-AR-000025090

Other devices from Suzhou Pelement Medical Technology Co., Ltd.

See all devices from Suzhou Pelement Medical Technology Co., Ltd. →

Properties

  • Reusable
  • Contains Latex YesEUDAMEDNoEUDAMED

Other properties (11)

  • Sterile: No
  • Implantable: 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