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Hilbro

by HILBRO International (Pvt) Ltd. 1,000+ variants

Ref 18.0012.10

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-G2781800121001 Basic UDI-DI G2781800121001UDI-DIDate21 Oct 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  • Withdrawn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
Farabeuf Retractor D/E set/2, 20x16mmx23x16mm 24x16mmx28x16mm, 15cm
Model / Reference
18.0012.10
Primary DI / UDI-DI
G2781800121001
Basic UDI-DI
B-G2781800121001
EMDN Code
L03140199 Spreaders and retractors for general surgery, reusable - other
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
PK-MF-000025041
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Hilbro International (Pvt) Limited

See all devices from Hilbro International (Pvt) Limited →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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