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Prepidil Gel Catheter

by Pfizer Manufacturing Belgium NV

Ref H000037140 OTH-CATHETER BLISTER ST. PAA236038 UNIV

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 Number5415062PPU5N04734D Basic UDI-DI 15415062394820UDI-DIDate10 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  • Withdrawn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
Endocervical Catheter (Sterile)
Model / Reference
H000037140 OTH-CATHETER BLISTER ST. PAA236038 UNIV
Primary DI / UDI-DI
15415062394820
Basic UDI-DI
5415062PPU5N04734D
EMDN Code
U080199 Gynaecological catheters - other
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
BE-MF-000003721

Other devices from Pfizer Manufacturing Belgium NV

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

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