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Polyethersulfone Hollow Fiber Hemodialyzers

by Allmed Middle East 23 variants

Ref HP 130 SModel HP 100 S HP 130 S HP 140 S HP 160 S HP 180 S HP 200 S HP 220 S HPM 100 S HPM 130 S HPM 160 S HPM 180 S HPM 200 S HPM 220 S, HP 100 S HP 130 S HP 140 S HP 160 S HP 180 S HP 200 S HP 220 S, HPM 100 S HPM 130 S HPM 160 S HPM 180 S HPM 200 S HPM 220 S

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6221166PESSTHDXV Basic UDI-DI Date15 Jun 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
Polyethersulfone Hollow Fiber Hemodialyzers
Model / Reference
HP 100 S HP 130 S HP 140 S HP 160 S HP 180 S HP 200 S HP 220 S HPM 100 S HPM 130 S HPM 160 S HPM 180 S HPM 200 S HPM 220 S, HP 130 S, HP 100 S HP 130 S HP 140 S HP 160 S HP 180 S HP 200 S HP 220 S, HPM 100 S HPM 130 S HPM 160 S HPM 180 S HPM 200 S HPM 220 S
Primary DI / UDI-DI
06221166000251, 06221166000244
Basic UDI-DI
6221166PESSTHDXV, 6221166PESRHDST
Direct Marketing DI
06221166000251
06221166000244
EMDN Code
F01060103 DIALYSERS - UFC < 18 ml/h/mmHg, SYNTHETIC MEMBRANES
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
EG-MF-000025747
Authorised representative
Allmed Medical GmbH DE-AR-000007830

Other devices from Allmed Middle East

See all devices from Allmed Middle East →

Properties

  • Sterile

Other properties (12)

  • 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