Plasti̇-Med

by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti. 310 variants

Ref 160 202 2 3 4

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08698573030801 Basic UDI-DI 08698573030801UDI-DI	Date3 Mar 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Withdrawn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: SUCTION BAG 1500ML W/O TUBE and W/ DISINFECTANT, GEL
Model / Reference: 160 202 2 3 4

Primary DI / UDI-DI: 08698573030801
Basic UDI-DI: B-08698573030801
EMDN Code: A060301 Collection bags and other containers for drainages and fistulas, single use

Device Class: Class IIa
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000032251

Other devices from Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.

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Plasti-Med

Class I
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Class IIa
Plasti-Med

Class I
Plasti-Med

Class I
Plasti-Med

Class I

See all devices from Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti. →

Properties

Measuring Function

Other properties (10)

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