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Aseltech

by Asel Tibbi Aletler A.S. 1,000+ variants

Ref CN-5233Model ASELTECH

Active European Union

CE MDR

Valid until

No date given

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 10 Nov 2026. What this means

Regulatory status

as of registry sync 10 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8681376ASELTECH201529AX Basic UDI-DI 08681376091452UDI-DIDate21 Dec 2023RegisteredStatusActive

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  • Withdrawn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
Sterilization Container Systems
Model / reference
ASELTECH, CN-5233
Primary DI / UDI-DI
08681376091452
Basic UDI-DI
8681376ASELTECH201529AX
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
Device class
Class I
EU registration type
Standard device
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019723

Overview

AI-generated summary, 10 Nov 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

ASELTECH is a sterilization container system, as indicated by its device type name. It is listed under EU MDR registration with Class I status, model ASELTECH, and reference CN-5233.

Other devices from Asel Tibbi Aletler A.S.

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Properties

  • Sterilise before use
  • Reusable

Other properties (12)

  • Supplied sterile: No
  • Implantable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No