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octenisan set

by Schülke & Mayr GmbH 3 variants

Ref 70003064

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4032651BSC00000046AJ Basic UDI-DI 04032651980659UDI-DIDate6 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
70003064
Primary DI / UDI-DI
04032651980659
Basic UDI-DI
4032651BSC00000046AJ
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class IIa
Medical Purpose
for preoperative decontamination of skin, hair and nasal vestubles

Manufacturer details

EUDAMED SRN
DE-PR-000039117

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Properties

Other properties (1)

  • Sterile: No