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Sterile Procedure Trays

by Medline International France 458 variants

Ref AGBNE056A

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3666520DCSPTNEUROSTIIIVF Basic UDI-DI 03666520407209UDI-DIDate27 Apr 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  • Withdrawn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

EU market availability

Not listed: EUDAMED names no country where this device is made available.

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

Last checked 2 Nov 2026.

Specification

EUDAMED

Device Name
Sterile Neurology procedure pack
Model / Reference
AGBNE056A
Primary DI / UDI-DI
03666520407209
Basic UDI-DI
3666520DCSPTNEUROSTIIIVF
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class III
Medical Purpose
For Neurology procedure

Manufacturer details

EUDAMED SRN
FR-PR-000003713

Other devices from Medline International France

See all devices from Medline International France →

Properties

  • Sterile