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Sterile Silicone Wound Drain- Perforated

by Medasil Surgical Limited 9 variants

Ref 410-1110-3216

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 Number506046556410-11BH Basic UDI-DI 05060465561930UDI-DIDate21 Mar 2025RegisteredStatusActive

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  • Withdrawn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
Sterile Silicone Wound Drain- Perforated
Model / Reference
410-1110-3216
Primary DI / UDI-DI
05060465561930
Basic UDI-DI
506046556410-11BH
Unit of Use DI
05060465561923
EMDN Code
A06010199 Vacuum and gravity drainage systems - other
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000009549
Authorised representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Other devices from Medasil Surgical Limited

See all devices from Medasil Surgical Limited →

Properties

  • Sterile

Other properties (12)

  • 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