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Permaflex Slides - White

by Leica Biosystems Richmond, Inc

Part of a family of 71 devices: see the family page

Ref 3800002

Permaflex Slides - White (3800002) is a Class A device made by Leica Biosystems Richmond, Inc, registered in EUDAMED on 23 Jul 2026 (Basic UDI-DI 849832003UK), active as of 8 Nov 2026.

Active European Union

CE IVDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number849832003UK Basic UDI-DI 10849832018688UDI-DIDate23 Jul 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device name
Slides
Model / reference
3800002
Primary DI / UDI-DI
10849832018688
Basic UDI-DI
849832003UK
Unit of use DI
00849832018681
EMDN code
W0599 IVD general use consumable devices - other
Device class
Class A
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000014614
Authorised representative
AR Experts B.V. NL-AR-000023989

Similar devices in this category

Other devices filed under IVD GENERAL USE CONSUMABLE DEVICES - OTHER.

Other devices from Leica Biosystems Richmond, Inc

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Properties

Other properties (13, all answered No)