A.C.A

by Ada Cerrahi̇ Aletler San. Ti̇c. Ltd. Şti̇. 1,000+ variants

Ref A.C.A 70102-17

Active European Union

CE MDD

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

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08680234091412 Basic UDI-DI 08680234091412UDI-DI	Date14 Oct 2026Registered	StatusActive

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

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Conservative
Model / Reference: A.C.A 70102-17

Primary DI / UDI-DI: 08680234091412
Basic UDI-DI: B-08680234091412
EMDN Code: L03130401 Tissue and organ grasping forceps, reusable

Device Class: Class I
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000029490

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Properties

Reusable

Other properties (10)

Sterile: No
Implantable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No