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HemaGel® SPRAY

by VH Pharma a.s. EUDAMED

Active European Union

Ref HS-30

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859417749HEMACUTSPRAYXQ Basic UDI-DIDate11 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 26 0172 QR/NB Issued

    Quality management system EU MDR

    Notified body
    Notified body 1023
    Issued
    30 Jun 2026
    Expires
    29 Jun 2031

Specification

EUDAMED

Device Name
Polymer spray
Model / Reference
HS-30
Primary DI / UDI-DI
08594177490617
Basic UDI-DI
859417749HEMACUTSPRAYXQ
EMDN Code
M04040701 Silicone dressings, non-combined
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000005951

Other devices from VH Pharma a.s.

See all devices from VH Pharma a.s. →

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