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Bss Plus

by Alcon Laboratories, Inc. 5 variants

Ref 0008200007

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number038065GMN000288HV Basic UDI-DI 20300650820077UDI-DIDate30 Mar 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  • Withdrawn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

Device Name
BSS PLUS Kit
Model / Reference
0008200007
Primary DI / UDI-DI
20300650820077
Basic UDI-DI
038065GMN000288HV
EMDN Code
Q02030203 Ophthalmic surgery balanced saline solutions
Device Class
Class IIa
Medical Purpose
The overall intended purpose of the procedure pack is to assist in the preparation of the BSS PLUS Solution.

Manufacturer details

EUDAMED SRN
US-PR-000037951

Other devices from Alcon Laboratories, Inc.

See all devices from Alcon Laboratories, Inc. →

Properties

  • Sterile