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Hemocor

by J Ripoll Sl 2 variants

Ref HEM

Hemocor is a medical device (EU MDD Class I; EMDN category retraction wires and gingival retractors) made by J Ripoll Sl, registered in EUDAMED on 6 May 2026 (Basic UDI-DI B-08436042240050), active as of 22 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08436042240050 Basic UDI-DI 08436042240050UDI-DIDate6 May 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
HEM
Primary DI / UDI-DI
08436042240050
Basic UDI-DI
B-08436042240050
EMDN code
Q010204 Retraction wires and gingival retractors
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001256

Similar devices in this category

Other devices filed under RETRACTION WIRES AND GINGIVAL RETRACTORS.

Other devices from J Ripoll Sl

See all devices from J Ripoll Sl →

Properties

Other properties (12, all answered No)