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Wiotech HA MD double 20 mg/mL volume&lines

by Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.

Ref HAMD2Model HAMD 2

Active European Union

CE MDD

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/MDD NumberB-843655523215G8XC Basic UDI-DI Date18 Feb 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
HAMD 2 20 mg/mL
HAMD double 20 mg/mL
Model / Reference
HAMD 2, HAMD2
Primary DI / UDI-DI
D-843655523215G8XC, 08436555230357
Basic UDI-DI
B-843655523215G8XC, B-08436555230357
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001065

Other devices from Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.

Properties

  • Sterile
  • Implantable
  • Reprocessed NoEUDAMEDYesEUDAMED

Other properties (8)

  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No