Aesculap

by Aesculap AG 718 variants

Ref JK389Y

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number4039239000001151ZR Basic UDI-DI 04038653330607UDI-DI	Date4 Jul 2025Registered	StatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name: Container
Model / Reference: JK389Y

Primary DI / UDI-DI: 04038653330607
Basic UDI-DI: 4039239000001151ZR
Direct Marketing DI: 04038653330607
EMDN Code: S010401 Trays, baskets, tubs for sterilisation and their components

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000005504

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Prevision

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Targon Pft

Class I
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Class I

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No