Vacusera

by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. 217 variants

Ref 235806

Active European Union

CE IVDR CE IVDD

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/IVDR	NumberB-M7122358061 Basic UDI-DI	Date2 Aug 2023Registered	StatusActive
European Union	CE/IVDD	NumberB-M7122358061 Basic UDI-DI	Date2 Aug 2023Registered	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Withdrawn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/IVDR, CE/IVDD Active

Specification

EUDAMED

Device Name: VACUSERA® 6 ml Z No Additive Urine Tube
VACUSERA® Urine Tubes
Model / Reference: 235806

Primary DI / UDI-DI: M7122358061, +M7122358061C
Basic UDI-DI: B-M7122358061, ++M712235URINETUBEX3
Direct Marketing DI: +M7122358061C
EMDN Code: W050101010201, W05010202

Device Class: Class IVD General
Class A
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000025066

Other devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş.

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Class A
Vacusera

Class A
Vacusera

Class A
Vacusera

Class A
Vacusera

Class A
Vacusera

Class A

See all devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. →

Properties

Sterile

Other properties (10)

Human Tissues: No
Animal Tissues: No
Microbial Substances: No
Reagent: No
Self Testing: No
Near-Patient Testing: No
Professional Testing: No
Companion Diagnostics: No
Surgical Instrument: No
New Device: No