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RowePhob 25/0.1 - RowePhob 25/0.1

by RoweMed AG - Medical 4 Life

Ref A-6375, A-6350

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42503476PHOB25DJ Basic UDI-DI Date4 Apr 2022RegisteredStatusActive

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  • Withdrawn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

Trade Name
RowePhob 25/0.1; 0,1 µm PTFE-Membran; LLw/LLm
RowePhob 25/0.1
Device Name
RowePhob
Model / Reference
A-6375, A-6350
Primary DI / UDI-DI
04250347603631, 04250347604980
Basic UDI-DI
42503476PHOB25DJ
EMDN Code
A04010101 Withdrawl and administration filters (0.2-1.2 microns)
Models / Variants
RowePhob 25/0.1
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005350

Other devices from RoweMed AG - Medical 4 Life

See all devices from RoweMed AG - Medical 4 Life →

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