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Surgical procedure kit, Anaesthesia

by Bastos Viegas S.A.

Ref 4905-885Model Sterile packs/sets/kits - Class III

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56056221255004LA Basic UDI-DI 05605622076706UDI-DIDate2 Nov 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
Sterile packs/sets/kits - Class III, 4905-885
Primary DI / UDI-DI
05605622076706
Basic UDI-DI
56056221255004LA
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class III
Medical Purpose
Intended to provide, in a single pack, the single-use medical device components required for a specific surgical or clinical procedure. Its designation expresses the particular intended purpose (surgical specialty/ clinical procedure)

Manufacturer details

EUDAMED SRN
PT-PR-000002808

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Properties

  • Sterile